Esters-buliding-blocks

Reversible addition-fragmentation chain transfer copolymerization of methyl methacrylate and methyl acrylate was written by Ionychev, B. N.;Semchikov, Yu. D.;Kopylova, N. A.;Andreeva, E. S.;Zaitsev, S. D.. And the article was included in Russian Journal of Applied Chemistry in 2014.Quality Control of Benzyl benzodithioate This article mentions the following:

Pseudo-living radical copolymerization of Me methacrylate and Me acrylate under reversible addition-fragmentation chain transfer in a mass in the presence of reversible chain transfer agents of different nature was implemented. A comparison of phys. and mech. properties of narrowly dispersed copolymers was performed as well as copolymers obtained by uncontrolled radical polymerization In the experiment, the researchers used many compounds, for example, Benzyl benzodithioate (cas: 27249-90-7Quality Control of Benzyl benzodithioate).

Benzyl benzodithioate (cas: 27249-90-7) 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. Polyesters are important plastics, with monomers linked by ester moieties. 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.Quality Control of Benzyl benzodithioate

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

Extraction, chemical composition, and anticancer potential of Origanum onites L. essential oil was written by Spyridopoulou, Katerina;Fitsiou, Eleni;Bouloukosta, Eleni;Tiptiri-Kourpeti, Angeliki;Vamvakias, Manolis;Oreopoulou, Antigoni;Papavassilopoulou, Eleni;Pappa, Aglaia;Chlichlia, Katerina. And the article was included in Molecules in 2019.Computed Properties of C6H12O2 This article mentions the following:

Origanum species are plants rich in volatile oils that are mainly used for culinary purposes. In recent years, there has been a growing interest in the biol. activities of their essential oils. Origanum onites L. is a plant mainly found in Greece, Turkey, and Sicily, whose oil is rich in carvacrol, a highly bioactive phytochem. The aim of this study was to analyze the chem. composition of Origanum onites essential oil (OOEO), and investigate its potential anticancer effects in vitro and in vivo. GC/MS anal. identified carvacrol as OOEO’s main constituent. In vitro antiproliferative activity was assayed with the sulforhodamine B (SRB) assay against human cancer cell lines from four tumor types. HT-29, a colorectal cancer cell line, was the most sensitive to the antiproliferative activity of OOEO. Wound-healing assay and Annexin V-PI staining were employed to investigate the antimigratory and the pro-apoptotic potential of OOEO, resp., against human (HT-29) and murine (CT26) colon cancer cells. Notably, OOEO attenuated migration and induced apoptosis-related morphol. changes in both cell lines. Prophylactic oral administration of the oil in a BALB/c exptl. mouse model inhibited the growth of syngeneic CT26 colon tumors. As far as we know, this is the first report on the antitumor potential of orally administered OOEO. In the experiment, the researchers used many compounds, for example, Methyl2-methylbutyrate (cas: 868-57-5Computed Properties of C6H12O2).

Methyl2-methylbutyrate (cas: 868-57-5) 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. 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.Computed Properties of C6H12O2

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

Modifications in Lemongrass (Cymbopogon spp.) in response to green synthesized nano-selenium complex was written by Tavallali, Vahid;Shabanpisheh, Zahra;Gholami, Hossein;Abarghuei, Faezeh Mirazimi. And the article was included in Scientia Horticulturae (Amsterdam, Netherlands) in 2022.Related Products of 105-87-3 This article mentions the following:

Selenium nanoparticles (Se-NPs) have different applications in various technologies due to their individual properties. In order to investigate the impacts of different concentrations of a green-synthesized selenium nano-complex (0, 20, 40, 60, and 80 mg L-1) on the chem. composition, antioxidant capacity and antimicrobial activity of lemongrass essential oil (EO), an experiment was designed as a completely randomized design (CRD) with four replications. The application of 40 mg L-1 selenium nano-complex caused the highest EO yield (3.96 鍗?0.09%). The dominant compounds in EO, geranial (44.12 鍗?1.22%) and neral (32.53 鍗?1.08%), were achieved by the application of 60 mg L-1 selenium nano-complex. HPLC anal. indicated that the extracts were rich in 5-o-cafeoylquinic acid, luteolin 6-c-pentosyl-8-c-pentoside, and luteolin 2-o-deoxyhexosyl-6-c-glucoside. The extracts of lemongrass plants treated with 40 and 60 mg L-1 selenium nano-complex achieved the highest amount of 5-o-cafeoylquinic acid (25.29鍗?.31 and 24.16鍗?.26 娓璯 mL-1, resp.). The highest antioxidant capacity was observed in the 40 mg L-1 selenium nano-complex treated plants. The min. inhibitory concentration (MIC) of EO derived from the 60 mg L-1 selenium nano-complex treated lemongrass for Salmonella typhimurium, Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Aspergillus niger and Candida albicans was 0.63鍗?.03, 1.84鍗?.1, 1.05鍗?.05, 0.008鍗?.01, 0.6鍗?.01 and 0.1鍗?.01 mg mL-1, resp. It is expected that the selenium nano-complex would find a wide range of applications in medicine for its antioxidant and antimicrobial properties. It may also be applied to medicinal plants to enhance the quality and quantity of EOs. In the experiment, the researchers used many compounds, for example, (E)-3,7-Dimethylocta-2,6-dien-1-yl acetate (cas: 105-87-3Related Products of 105-87-3).

(E)-3,7-Dimethylocta-2,6-dien-1-yl acetate (cas: 105-87-3) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Related Products of 105-87-3

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

Synthesis of 1,1-[1-Naphthyloxy-2-thiophenyl]-2-methylaminomethylcyclopropanes and their Evaluation as Inhibitors of Serotonin, Norepinephrine, and Dopamine Transporters was written by White, James D.;Juniku, Rajan;Huang, Kun;Yang, Jongtae;Wong, David T.. And the article was included in Journal of Medicinal Chemistry in 2009.Safety of Ethyl 3-oxo-3-(thiophen-2-yl)propanoate This article mentions the following:

Stereodefined trisubstituted cyclopropanes I bearing naphthyloxy, thiophenyl, and (N-methylamino)methyl groups were synthesized in enantiopure form employing asym. cyclopropanation of (E)- and (Z)-allylic alcs. as the key step. In vitro assays of the synthesized cyclopropanes revealed that the K_i of one of the enantiomers as a dual inhibitor of serotonin and norepinephrine transporters is in the low nanomolar range and is comparable to that of duloxetine. In the experiment, the researchers used many compounds, for example, Ethyl 3-oxo-3-(thiophen-2-yl)propanoate (cas: 13669-10-8Safety of Ethyl 3-oxo-3-(thiophen-2-yl)propanoate).

Ethyl 3-oxo-3-(thiophen-2-yl)propanoate (cas: 13669-10-8) 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. 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.Safety of Ethyl 3-oxo-3-(thiophen-2-yl)propanoate

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

Isovaleronitrile co-induced with its precursor, L-leucine, by herbivory in the common evening primrose stimulates foraging behavior of the predatory blue shield bug was written by Noge, Koji;Tamogami, Shigeru. And the article was included in Bioscience, Biotechnology, and Biochemistry in 2018.Category: esters-buliding-blocks This article mentions the following:

Herbivore-induced plant volatiles play important roles in plant-insect and plant-plant interactions. The common evening primrose, Oenothera biennis, is often infested by the flea beetle, Altica oleracea, on which the predatory blue shield bug, Zicrona caerulea, is usually found. This observation suggests that the predatory bug can discriminate infested plants from intact ones to locate its prey. In this study, L-leucine-derived nitrogen-containing compounds [isovaleronitrile (3-methylbutanenitrile), (E/Z)-isovaleraldoxime and 3-methyl-1-nitrobutane] and some terpenes were identified as a characteristic volatile blend from herbivore-infested O. biennis leaves by gas chromatog./mass spectrometry, chem. synthesis, and incorporation assays using deuterium-labeled L-leucine. Volatile emission was also elicited by exogenous Me jasmonate (MeJA), but not by mech. damage. L-Leucine accumulated temporarily in O. biennis leaves after MeJA treatment prior to isovaleronitrile emission. Behavioral assays revealed that Z. caerulea showed a strong preference for herbivore-infested leaves, their volatiles, and isovaleronitrile in laboratory conditions. In the experiment, the researchers used many compounds, for example, Isopentyl 3-methylbutanoate (cas: 659-70-1Category: esters-buliding-blocks).

Isopentyl 3-methylbutanoate (cas: 659-70-1) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. 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.Category: esters-buliding-blocks

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

Enantiomer separation of mandelates and their analogs on cyclodextrin derivative chiral stationary phases by capillary GC was written by Nie, Meng-Yan;Zhou, Liang-Mo;Wang, Qing-Hai;Zhu, Dao-Qian. And the article was included in Analytical Sciences in 2001.Related Products of 15399-05-0 This article mentions the following:

Enantiomer separation of mandelates and their analogs, which are important intermediates in asym. synthetic and pharmaceutical chem., was studied by capillary gas chromatog. using different cyclodextrin derivative chiral stationary phases (CD CSPs). The used cyclodextrin derivatives included permethylated 灏?CD (PMBCD), permethylated 绾?CD, heptakis(2,6-di-O-butyl-3-O-butyryl)-灏?CD, heptakis(2,6-di-O-pentyl-3-O-acetyl)-灏?CD and heptakis(2,6-di-O-nonyl-3-O-trifluoroacetyl)-灏?CD (DNTBCD), resp. Among all the CSPs used, PMBCD and DNTBCD exhibited the broadest and best enantioselectivity for all the racemates studied. Some thermodn. parameters were evaluated and an enthalpy-entropy compensation effect was observed in enantiomer separation processes of mandelates and their analogs. Based on thermodn. data and mol. mechanics calculations, the chiral recognition mechanism of mandelate derivatives on CD CSPs is discussed. In the experiment, the researchers used many compounds, for example, Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0Related Products of 15399-05-0).

Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) 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. 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.Related Products of 15399-05-0

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

Changes in free and glycosidically bound volatile compounds of nectarine fruit during low-temperature storage was written by Zhang, Q.;Zhou, D. D.;Jiang, M. W.;Tu, K.. And the article was included in International Food Research Journal in 2022.Recommanded Product: 5-Ethyldihydrofuran-2(3H)-one This article mentions the following:

Free and glycosidically bound volatiles are two essential aroma compounds contributing to the flavor of nectarine fruits. To explore the relationship between free and bound volatiles in nectarine fruits during postharvest storage, they were first harvested and then subjected to the temperatures of 1, 5, and 8鎺矯 for 35 d, and the changes in volatile compounds, 灏?glucosidase (灏?Glu) activity, and the expression of UGT (UDP-glucosyltransferase) involved in the accumulation of bound linalool were determined Results showed that nectarine fruits stored at 5鎺矯 had the lowest contents of free volatile compounds due to damage from chilling injury, and the contents of esters and lactones decreased at 1 and 5鎺矯. The contents of bound volatiles increased during the early storage period, and decreased afterwards due to an increase in 灏?Glu activity. Corresponding to the higher contents of bound volatiles at 1鎺矯, the 灏?Glu activity in nectarine fruits stored at 1鎺矯 was significantly lower than that in nectarine fruits stored at the other two temperatures In the experiment, the researchers used many compounds, for example, 5-Ethyldihydrofuran-2(3H)-one (cas: 695-06-7Recommanded Product: 5-Ethyldihydrofuran-2(3H)-one).

5-Ethyldihydrofuran-2(3H)-one (cas: 695-06-7) 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.Recommanded Product: 5-Ethyldihydrofuran-2(3H)-one

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

Chemical composition and oxidative stability of eleven pecan cultivars produced in southern Brazil was written by Reis Ribeiro, Stephanie;Klein, Bruna;Machado Ribeiro, Quellen;Duarte dos Santos, Ingrid;Gomes Genro, Ana Luisa;de Freitas Ferreira, Daniele;Janner Hamann, Jonas;Smanioto Barin, Juliano;Cichoski, Alexandre Jose;Fronza, Diniz;Both, Vanderlei;Wagner, Roger. And the article was included in Food Research International in 2020.Category: esters-buliding-blocks This article mentions the following:

Nuts are considered highly nutritious foods and a source of health-promoting compounds Therefore, the aim of this study was to evaluate the chem. composition (proximate composition, fatty acids, volatile compounds, total phenolics, squalene, and 灏?sitosterol) of eleven pecan cultivars harvested in Rio Grande do Sul State (Brazil) and investigate their oxidative stability by the Rancimat method. ‘Barton’ is the main cultivar produced in Brazil and presented the highest protein, linoleic acid, and linolenic acid values and the lowest saturated fatty acid values, which provide health benefits. ‘Mahan’ showed the highest oxidation induction time, both in extracted oil and ground samples, low abundance of lipid oxidation compounds, low polyunsaturated fatty acids, high levels of oleic acid and 灏?sitosterol, which suggests potential for storage. ‘Stuart’ and ‘Success’ had the highest total dietary fiber values. Moreover, anal. showed that ‘Chickasaw’ and ‘Success’ had large quantities of compounds correlated to lipid oxidation, suggesting low stability for long-term storage. These results imply that the physicochem. characteristics and proximate composition of pecan nut cultivars from southern Brazil have variable parameters that may depend on their genetic variability. In the experiment, the researchers used many compounds, for example, 5-Ethyldihydrofuran-2(3H)-one (cas: 695-06-7Category: esters-buliding-blocks).

5-Ethyldihydrofuran-2(3H)-one (cas: 695-06-7) 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. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Category: esters-buliding-blocks

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

浼?Ketoamide Phe-Pro isostere as a new core structure for the inhibition of HIV protease was written by Munoz, Benito;Giam, Chou-Zen;Wong, Chi-Huey. And the article was included in Bioorganic & Medicinal Chemistry in 1994.Name: (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate This article mentions the following:

Studies on the inhibition of HIV-1 protease utilizing a core isostere with replacement of the scissile bond for an 浼?amino-ketone have resulted in the development of an 浼?keto-amide isosteric replacement of the Phe-Pro scissile amide bond. The simple dipeptide isostere I was a promising new core structure for the development of the enzyme inhibitors. I exhibited K_i = 6 娓璏 against HIV-1 protease, compared to 230 娓璏 and >50 娓璏 for the corresponding phosphinic acid and hydroxyethylamine isosteres. 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: 87694-53-9Name: (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate).

(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. Esters contain a carbonyl center, which gives rise to 120鎺?C閳ユ弲閳ユ彊 and O閳ユ弲閳ユ彊 angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C閳ユ彊閳ユ弲 bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Name: (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate

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

An expedient conversion of 浼?amino acids into Weinreb amides using COMU as a coupling agent was written by Tyrrell, Elizabeth;Brawn, Peter;Carew, Mark;Greenwood, Iain. And the article was included in Tetrahedron Letters in 2011.Product Details of 87694-53-9 This article mentions the following:

The use of COMU, as a non-hazardous partner, in the coupling of N-Boc 浼?amino acids with N-methoxy-N-methylamine to afford the corresponding Weinreb amides is discussed. From a practical point of view the reaction can be monitored visually by virtue of the color change associated with the conversion of substrates (yellow) into the products (orange). As the byproducts of the reaction are conveniently water-soluble, the products are isolated relatively pure and with minimal racemization. These factors coupled with the short reaction time make this a very useful procedure. 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: 87694-53-9Product Details 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. 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.Product Details of 87694-53-9

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