Hu, Xi-Le et al. published their research in Advanced Functional Materials in 2019 | CAS: 4163-60-4

(2S,3R,4S,5S,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 4163-60-4) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Category: esters-buliding-blocks

Multivalent Glycosheets for Double Light-Driven Therapy of Multidrug-Resistant Bacteria on Wounds was written by Hu, Xi-Le;Chu, Linyang;Dong, Xiaojing;Chen, Guo-Rong;Tang, Tingting;Chen, Daijie;He, Xiao-Peng;Tian, He. And the article was included in Advanced Functional Materials in 2019.Category: esters-buliding-blocks This article mentions the following:

With the evergrowing threat posed by multidrug resistance of bacteria, the development of effective antibacterial agents remains a global challenge. Infection with multidrug-resistant bacteria in hospitals significantly impairs the healing of wounds caused by deep-burn injuries or diabetic foot ulceration, leading to a high mortality rate among these patients. A multivalent glycosheet for the double light-driven therapy against multidrug-resistant Pseudomonas aeruginosa (P. aeruginosa) infection on wounds is developed here. Galactose- and fucose-based ligands are self-assembled to form a glyco-layer on the surface of thin-layer molybdenum disulfide, producing the glycosheets capable of selectively localizing P. aeruginosa through multivalent carbohydrate-lectin interactions. The glycosheets loaded with antibiotics have proven applicable for: (1) near-IR-light driven, in situ thermal release of antibiotics, increasing bacterial membrane permeability, and (2) white light-driven reactive-oxygen-species production to more thoroughly kill the bacteria. The targetability, together with the light sensibility, of the glycosheets enables a highly effective and optically controlled therapeutic regime for the healing of wounds infected by multidrug-resistant as well as clin. isolated P. aeruginosa. In the experiment, the researchers used many compounds, for example, (2S,3R,4S,5S,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 4163-60-4Category: esters-buliding-blocks).

(2S,3R,4S,5S,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 4163-60-4) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Belleggia, Luca et al. published their research in Food Research International in 2022 | CAS: 695-06-7

5-Ethyldihydrofuran-2(3H)-one (cas: 695-06-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Computed Properties of C6H10O2

Unravelling microbial populations and volatile organic compounds of artisan fermented liver sausages manufactured in Central Italy was written by Belleggia, Luca;Ferrocino, Ilario;Reale, Anna;Haouet, M. Naceur;Corvaglia, Maria Rita;Milanovic, Vesna;Boscaino, Floriana;Di Renzo, Tiziana;Di Bella, Sara;Borghi, Monica;Farneti, Silvana;Cesaro, Cristiana;Garofalo, Cristiana;Cardinali, Federica;Aquilanti, Lucia;Musari, Evan;Cocolin, Luca;Osimani, Andrea. And the article was included in Food Research International in 2022.Computed Properties of C6H10O2 This article mentions the following:

The aim of the present study was to obtain information on the occurrence of bacteria and eumycetes in ready-to-eat fermented liver sausages manufactured by 20 artisan producers located in the Marche Region (Italy). To this end, culture-dependent analyses and metataxonomic sequencing were carried out. Physico-chem. parameters and volatilome of the fermented liver sausages were also studied. Finally, the presence of hepatitis E virus (HEV) was also assessed via real-time-RT-(q)PCR assays. Active microbial populations mainly represented by lactic acid bacteria, enterococci, coagulase-neg. cocci, and eumycetes were detected. Enterobacteriaceae, Pseudomonadaceae, and sulfite-reducing anaerobes were not detected in most of the samples. Latilactobacillus sakei dominated in all the analyzed samples, reaching abundances up to 80%. Staphylococcus xylosus and Staphylococcus equorum were also detected. Among minority bacterial taxa, Weissella spp., Leuconostoc spp., Macrococcus caseolyticus, Brochothrix thermosphacta, Staphylococcus succinus, Lactobacillus coryniformis, Lactiplantibacillus plantarum, Lactococcus garviae, Psychrobacter spp., and Carnobacterium viridans were detected. The mycobiota was mainly composed by Debaryomyces hansenii that was present in all samples at the highest frequency. Among minority fungal taxa, Aspergillus spp., Penicillium spp., Kurtzmaniella zeylanoides, Candida spp., Yamadazyma spp., Scopulariopsis spp., Yarrowia spp., and Starmerella spp. were detected. Interestingly, associations between some taxa and some physico-chem. parameters were also discovered. The absence of HEV in all the samples attested a high level of safety. Finally, most of the VOCs detected in the analyzed fermented liver sausages belonged to six classes as: terpenoids, aldehydes, ketones, alcs., esters, and acids. Nitrogen compounds, sulfur compounds, phenols, hydrocarbons, lactones, furans, and aromatic hydrocarbons were also identified. Several significant relationships were observed between mycobiota and VOCs. In the experiment, the researchers used many compounds, for example, 5-Ethyldihydrofuran-2(3H)-one (cas: 695-06-7Computed Properties of C6H10O2).

5-Ethyldihydrofuran-2(3H)-one (cas: 695-06-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Computed Properties of C6H10O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Modranka, Jakub et al. published their research in ChemMedChem in 2019 | CAS: 16413-26-6

3-Cyanophenylisocyanate (cas: 16413-26-6) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Related Products of 16413-26-6

Synthesis and Structure-Activity Relationship Studies of Benzo[b][1,4]oxazin-3(4H)-one Analogues as Inhibitors of Mycobacterial Thymidylate Synthase X was written by Modranka, Jakub;Li, Jiahong;Parchina, Anastasia;Vanmeert, Michiel;Dumbre, Shrinivas;Salman, Mayla;Myllykallio, Hannu;Becker, Hubert F.;Vanhoutte, Roeland;Margamuljana, Lia;Nguyen, Hoai;Abu El-Asrar, Rania;Rozenski, Jef;Herdewijn, Piet;De Jonghe, Steven;Lescrinier, Eveline. And the article was included in ChemMedChem in 2019.Related Products of 16413-26-6 This article mentions the following:

Since the discovery of a flavin-dependent thymidylate synthase (ThyX or FDTS) that is absent in humans but crucial for DNA biosynthesis in a diverse group of pathogens, the enzyme has been pursued for the development of new antibacterial agents against Mycobacterium tuberculosis, the causative agent of the widespread infectious disease tuberculosis (TB). In response to a growing need for more effective anti-TB drugs, we have built upon our previous screening efforts and report herein an optimization campaign of a novel series of inhibitors with a unique inhibition profile. The inhibitors display competitive inhibition toward the methylene tetrahydrofolate cofactor of ThyX, enabling us to generate a model of the compounds bound to their target, thus offering insight into their structure-activity relationships. In the experiment, the researchers used many compounds, for example, 3-Cyanophenylisocyanate (cas: 16413-26-6Related Products of 16413-26-6).

3-Cyanophenylisocyanate (cas: 16413-26-6) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Related Products of 16413-26-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Johansson, Patrik G. et al. published their research in Inorganic Chemistry in 2013 | CAS: 313648-56-5

Dimethyl 5-ethynylisophthalate (cas: 313648-56-5) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Formula: C12H10O4

Homoleptic “Star” Ru(II) Polypyridyl Complexes: Shielded Chromophores to Study Charge-Transfer at the Sensitizer-TiO2 Interface was written by Johansson, Patrik G.;Zhang, Yongyi;Meyer, Gerald J.;Galoppini, Elena. And the article was included in Inorganic Chemistry in 2013.Formula: C12H10O4 This article mentions the following:

Three homoleptic star-shaped Ru polypyridyl complexes, termed Star YZ1, Star YZ2, and Star YZ3, where the Ru(II) center is coordinated to three bipyridine ligands each carrying two oligo(phenylene ethynylene) (OPE) rigid linker units terminating with isophthalic ester (Ipa) groups for binding to metal-oxide surfaces were synthesized. In Star YZ3, each OPE linker was substituted with two n-butoxy (BuO) solubilizing groups. Star complex YZ4, which is homoleptic but lacks the octahedral symmetry, was synthesized as a reference compound The Star complexes were synthesized using two approaches: in the first, Ru(4,4′-(Br)2-2,2′-bpy)3 was reacted in a Sonogashira cross coupling reaction with the ethynyl-OPE-Ipa linkers; in the second, the 2,2′-bpy-OPE-Ipa ligands were reacted with Ru(DMSO)4(PF6)2. The photophys. behavior of the Star complexes were studied in fluid solution and anchored to the surface of mesoporous nanocrystalline TiO2 thin films (Star/TiO2). To a first approximation the excited state behavior in MeCN was unchanged when the compounds were anchored to a TiO2 thin film, indicating that the highly sym. (octahedral) and rigid mol. structure of the ligands shielded the chromophoric core from the TiO2 semiconductor. Inefficient excited state injection, φinj < 0.05, occurs on a nanosecond time scale with slow recombination. The presence of BuO groups on the linker unit gave a large increase in the extinction coefficient of YZ3, which allows for enhanced harvesting of sunlight. Mol. design on the nanometer length scale can be used to control excited state relaxation pathways at semiconductor surfaces. In the experiment, the researchers used many compounds, for example, Dimethyl 5-ethynylisophthalate (cas: 313648-56-5Formula: C12H10O4).

Dimethyl 5-ethynylisophthalate (cas: 313648-56-5) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Formula: C12H10O4

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Murray, William V. et al. published their research in Tetrahedron Letters in 2002 | CAS: 87694-53-9

(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate (cas: 87694-53-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Related Products of 87694-53-9

Synthesis of densely functionalized pyrrolidinone templates by an intramolecular oxo-Diels-Alder reaction was written by Murray, William V.;Mishra, Pranab K.;Sun, Sengen;Maden, Amy. And the article was included in Tetrahedron Letters in 2002.Related Products of 87694-53-9 This article mentions the following:

Preparation of densely functionalized pyrrolidinone templates, is a challenge for synthetic chemists. These templates are important building blocks for novel conformationally constrained natural products or for library generation of highly functionalized bi or polycyclic compounds Trienes, e.g. I, undergo facile stereoselective intramol. Diels Alder reactions to generate densely functionalized cis fused pyrrolidinone templates, e.g. II. These reactions allow for directed remote hydroxylation with complete control of stereochem. In the experiment, the researchers used many compounds, for example, (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate (cas: 87694-53-9Related Products of 87694-53-9).

(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate (cas: 87694-53-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Related Products of 87694-53-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Xu, Kai et al. published their research in Organic Letters in 2020 | CAS: 33166-79-9

Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Electric Literature of C12H14O3

Desymmetrization of meso-Dicarbonatecyclohexene with β-Hydrazino Carboxylic Esters via a Pd-Catalyzed Allylic Substitution Cascade was written by Xu, Kai;Zheng, Yan;Ye, Yong;Liu, Delong;Zhang, Wanbin. And the article was included in Organic Letters in 2020.Electric Literature of C12H14O3 This article mentions the following:

The desymmetrization of meso-dicarbonatecyclohexene with β-hydrazino carboxylic esters has been achieved via a RuPHOX/Pd-catalyzed allylic substitution cascade for the construction of chiral hexahydrocinnoline derivatives with high performance. Mechanistic studies reveal that the reaction exploits a pathway different from that of our previous work and that the first nitrogen nucleophilic process is the rate-determining step. The protocol could be conducted on a gram scale without any loss of catalytic behavior, and the corresponding chiral hexahydrocinnolines can undergo diverse transformations. In the experiment, the researchers used many compounds, for example, Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9Electric Literature of C12H14O3).

Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Electric Literature of C12H14O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Tanase, Shohjiroh et al. published their research in Journal of Molecular Catalysis A: Chemical in 2007 | CAS: 1190-39-2

malonic acid dibutyl ester (cas: 1190-39-2) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: malonic acid dibutyl ester

Design of novel malonates as internal donors for MgCl2-supported TiCl4 type polypropylene catalysts and their mechanistic aspects, Part 1 was written by Tanase, Shohjiroh;Katayama, Kiyokazu;Yabunouchi, Nobuhiro;Sadashima, Takanori;Tomotsu, Norio;Ishihara, Nobuhide. And the article was included in Journal of Molecular Catalysis A: Chemical in 2007.Recommanded Product: malonic acid dibutyl ester This article mentions the following:

Various malonate compounds (R1R2C(COOBu)2) with different substituents (R1, R2) were systematically synthesized and investigated for use as an internal donor (ID) in combination with a MgCl2-supported TiCl4 type catalyst, a triethylaluminum (TEA) co-catalyst and an alkoxysilane external donor (ED) for application in propylene polymerization The catalytic activity and isotacticity of polypropylene (PP) greatly depended on not only the oxygen electron d. of the ED, but also on the mol. volume of the ID. Furthermore, the mechanism of the active site formation was discussed with respect to the composition of the catalyst treated with TEA and ED, and with respect to the temperature rising elution fractionation (TREF) results of PP and so on. It was presumed that the desorption of malonates near Ti species from MgCl2 caused the generation of atactic PP sites, and the decrease of the isotacticity of PP. In the experiment, the researchers used many compounds, for example, malonic acid dibutyl ester (cas: 1190-39-2Recommanded Product: malonic acid dibutyl ester).

malonic acid dibutyl ester (cas: 1190-39-2) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: malonic acid dibutyl ester

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Snyder, Lawrence B. et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2004 | CAS: 2327-45-9

Methyl 5-methoxy-2-nitrobenzoate (cas: 2327-45-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.HPLC of Formula: 2327-45-9

Discovery of isoxazolinone antibacterial agents. Nitrogen as a replacement for the stereogenic center found in oxazolidinone antibacterials was written by Snyder, Lawrence B.;Meng, Zhaoxing;Mate, Robert;D’Andrea, Stanley V.;Marinier, Anne;Quesnelle, Claude A.;Gill, Patrice;DenBleyker, Kenneth L.;Fung-Tomc, Joan C.;Frosco, MaryBeth;Martel, Alain;Barrett, John F.;Bronson, Joanne J.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2004.HPLC of Formula: 2327-45-9 This article mentions the following:

A series of potential antimicrobial derivatives possessing bioisosteric replacements for the central oxazolidinone ring found in oxazolidinone antibacterials have been prepared The design concept involved replacement of the requisite sp3-hybridized stereogenic center found at the 5-position of the oxazolidinone with a nitrogen atom. The synthesis and antibacterial activity of three such ring systems, the benzisoxazolinones, e.g., I, pyrroles, e.g., II, and isoxazolinones, e.g., III, is described. In the experiment, the researchers used many compounds, for example, Methyl 5-methoxy-2-nitrobenzoate (cas: 2327-45-9HPLC of Formula: 2327-45-9).

Methyl 5-methoxy-2-nitrobenzoate (cas: 2327-45-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.HPLC of Formula: 2327-45-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Dikusar, E. A. et al. published their research in Russian Journal of Organic Chemistry in 2006 | CAS: 20665-85-4

4-Formyl-2-methoxyphenyl isobutyrate (cas: 20665-85-4) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Recommanded Product: 4-Formyl-2-methoxyphenyl isobutyrate

Preparative synthesis of {[4-hydroxy(alkyloyloxy, aryloyloxy)-3-methoxy(ethoxy)phenyl]methylene}(4-carboxyphenyl)amines was written by Dikusar, E. A.;Kozlov, N. G.;Zhukovskaya, N. A.;Potkin, V. I.;Ogorodnikova, M. M.;Zelenkovskii, V. M.. And the article was included in Russian Journal of Organic Chemistry in 2006.Recommanded Product: 4-Formyl-2-methoxyphenyl isobutyrate This article mentions the following:

By reactions of vanillin, vanillal, and their esters with 4-aminobenzoic acid in methanol formerly unknown E-isomers of azomethines (Schiff bases) were prepared In the experiment, the researchers used many compounds, for example, 4-Formyl-2-methoxyphenyl isobutyrate (cas: 20665-85-4Recommanded Product: 4-Formyl-2-methoxyphenyl isobutyrate).

4-Formyl-2-methoxyphenyl isobutyrate (cas: 20665-85-4) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Recommanded Product: 4-Formyl-2-methoxyphenyl isobutyrate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Zhang, Shuo et al. published their research in Journal of Food Processing and Preservation in 2022 | CAS: 706-14-9

5-Hexyldihydrofuran-2(3H)-one (cas: 706-14-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Related Products of 706-14-9

Changes in functional components and biological activity of Lycium barbarum after fermentation with Kombucha SCOBY was written by Zhang, Shuo;Tang, Yuxin;Chen, Julong. And the article was included in Journal of Food Processing and Preservation in 2022.Related Products of 706-14-9 This article mentions the following:

Kombucha, fermented via symbiotic colony of bacteria and yeast (SCOBY) with black tea, is applied as a nova microbial method for processing traditional Chinese medicine (TCM). In this study, Lycium barbarum was used as the substrate combined with Kombucha SCOBY to enhance its antioxidant activities and flavor composition The result indicated that the antioxidant activities of L. barbarum fermentation broth (LBF) was increased and 16.51% higher compared to the infusion. Besides, the inhibition zone of LBF on the 10th day against Escherichia coli and Staphylococcus aureus reached the maximum of 18.80 and 21.85 mm. Three typical L. barbarum polysaccharides, including LBP1, LBP2, and LBP3, were extracted and their compositions were identified. Among them, the DPPH scavenging rate and reducing power of LBP2 were 67.36% and 0.612 which were both higher than others. Furthermore, SOD enzyme and cellulase activity of LBF on 10th day were improved by 92.41% and 2.27 times, resp. Thirty-one aroma compounds were determined in Lycium barbarum Kombucha ferment via GC-MS. The strongest flavor of the LBF was sourness while the weakest flavor was saltiness which was analyzed through the electronic tongue. Our research provides a theor. basis for the development of functional L. barbarum Kombucha product and explores the application of Kombucha SCOBY in processing TCM. In the experiment, the researchers used many compounds, for example, 5-Hexyldihydrofuran-2(3H)-one (cas: 706-14-9Related Products of 706-14-9).

5-Hexyldihydrofuran-2(3H)-one (cas: 706-14-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Related Products of 706-14-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics