Zhang, Yu et al. published their research in Polymers for Advanced Technologies in 2022 | CAS: 6683-19-8

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) 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. 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.Application of 6683-19-8

Morphology evolution and mechanical property enhancement of linear low-density polyethylene by adding disentangled ultrahigh molecular weight polyethylene was written by Zhang, Yu;Di, Yutao;Ye, Chunlin;Zhang, Letian;Tang, Xin;Shu, Baoqiang;Yan, Xiang;Li, Wei;Wang, Jingdai;Yang, Yongrong. And the article was included in Polymers for Advanced Technologies in 2022.Application of 6683-19-8 This article mentions the following:

Ultra-high mol. weight polyethylene (UHMWPE) and linear low-d. polyethylene (LLDPE) with different ratios were melt-blended in an internal mixer. Results of rheol. tests and SEM indicate that the blends are well miscible in the range of small addition amount of UHMWPE. The content of UHMWPE is suggested to be less than 5.0 wt%, to guarantee good compatibility of biphasic blends. Differential scanning calorimetry studies indicate that co-crystallization occurs between UHMWPE and LLDPE. The crystallinity increases with the increase of UHMWPE as a nucleating agent. As a result, an improvement in mech. properties is achieved. When the addition amount of UHMWPE is 5.0 wt%, the impact strength, breaking elongation, Young’s modulus, and tensile strength are significantly increased by 27%, 25%, 75%, and 21% resp. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Application of 6683-19-8).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) 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. 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.Application of 6683-19-8

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

Arpa Zemzemoglu, Tuba Eda et al. published their research in European Food Research and Technology in 2021 | CAS: 15399-05-0

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

Enological properties of red wine produced from native Kosetevek grapes (Vitis vinifera L.) cultivated in Eastern Anatolia was written by Arpa Zemzemoglu, Tuba Eda;Darici, Merve;Cabaroglu, Turgut. And the article was included in European Food Research and Technology in 2021.SDS of cas: 15399-05-0 This article mentions the following:

The aim of this study was to determine the potential of red wine production from the Kosetevek grape variety (Vitis Vinifera L.) cultivated in Elazig province of Turkey and to define the characteristics of Kosetevek wines. To determine the grapes for wine production quality, the general composition, phenolic compounds, aroma compounds and sensory anal. of the wines were carried out. Aroma compounds were performed by solid-phase extraction (SPE) and then analyzed by gas chromatog. (GC) along with gas chromatog./mass spectrometry (GC/MS). Results showed that the red wines obtained from Kosetevek grapes consisted of 50 aroma compounds for 2014 vintages and 49 aroma compounds for 2015 vintages. Esters were the main components contributing to the Kosetevek wine aroma along with Et hydrogen succinate and ethyl-4-hydroxy butanoate. The amount of total phenolic compounds, total anthocyanin, and the tannin in Kosetevek wines were found to be between 3705.45 and 3015.63 mg/L, 554.25-502.35 mg/L, and 4.5-3.95 g/L at 2014-2015 vintages, resp. As to sensory evaluation, Kosetevek wines were characterized as a deep purple color, middle to high body, and rich in red fruit (cherries, plums), and dried fruit odors. This study has provided enol. properties and aroma characterization of Kosetevek wines. The results of the study showed that Kosetevek wines could be considered as an alternative to other wines obtained from native grape varieties of the region. In the experiment, the researchers used many compounds, for example, Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0SDS of cas: 15399-05-0).

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

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

Bach, Peter et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2011 | 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. 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 3-Cyanophenylisocyanate

A novel series of piperazinyl-pyridine ureas as antagonists of the purinergic P2Y12 receptor was written by Bach, Peter;Bostroem, Jonas;Brickmann, Kay;van Giezen, J. J. J.;Hovland, Ragnar;Petersson, Annika U.;Ray, Asim;Zetterberg, Fredrik. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2011.Quality Control of 3-Cyanophenylisocyanate This article mentions the following:

A novel series of P2Y12 antagonists for development of drugs within the antiplatelet area is presented. The synthesis of 2-(4-carbamoylpiperazinyl)pyridine-5-carboxylates and their structure-activity relationships (SAR) are described. Several compounds showed P2Y12 antagonistic activities in the sub-micromolar range. In the experiment, the researchers used many compounds, for example, 3-Cyanophenylisocyanate (cas: 16413-26-6Quality Control of 3-Cyanophenylisocyanate).

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. 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 3-Cyanophenylisocyanate

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

von Czapiewski, Marc et al. published their research in ACS Sustainable Chemistry & Engineering in 2018 | CAS: 106-79-6

Dimethyl decanedioate (cas: 106-79-6) 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.Application of 106-79-6

Fatty Acid Derived Renewable Platform Chemicals via Selective Oxidation Processes was written by von Czapiewski, Marc;Rhein, Michael;Meier, Michael A. R.. And the article was included in ACS Sustainable Chemistry & Engineering in 2018.Application of 106-79-6 This article mentions the following:

Highly efficient synthesis processes for the selective catalytic oxidation of unsaturated fatty acid Me esters (FAMEs) are described, leading to valuable renewable platform chems. Here keto-FAMEs derived from Me oleate and Me erucate were synthesized via a cocatalyst-free Wacker oxidation process using a high pressure reactor system. The catalytic system of palladium(II) chloride in dimethylacetamide/water enabled the oxidation of monounsaturated FAMEs in the presence of mol. oxygen as sole reoxidant with reduced amounts of solvent in shorter reaction time compared to previous reports. The high product selectivity is confirmed by two different synthesis approaches and the characterization of thereof derived products using mass spectrometry measurements (GC-MS, ESI-MS-MS). The obtained keto-FAMEs are used in a subsequent Baeyer-Villiger oxidations with m-CPBA, enabling the synthesis of diesters, thus allowing access to various platform chems. (e.g., hydroxy-esters, fatty alcs.). Moreover, an enone derivative, which can be obtained through selective photo peroxidation of Me oleate, is studied in the cocatalyst-free Wacker oxidation process leading to a 1,3-diketone. Addnl., the same enone is used in the Baeyer-Villiger oxidation with Oxone and m-CPBA as oxidant, allowing the highly selective synthesis of a vinyl acetate and an epoxy diester derivative, resp. In the experiment, the researchers used many compounds, for example, Dimethyl decanedioate (cas: 106-79-6Application of 106-79-6).

Dimethyl decanedioate (cas: 106-79-6) 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.Application of 106-79-6

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

Corona, Onofrio et al. published their research in Industrie delle Bevande in 2011 | CAS: 15399-05-0

Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.SDS of cas: 15399-05-0

White winemaking in the presence of oak chips of different origin and toasting level was written by Corona, Onofrio;de Filippi, Diego;Riccobono, Pietro;Plodari, Roberto;Scavone, Luigi. And the article was included in Industrie delle Bevande in 2011.SDS of cas: 15399-05-0 This article mentions the following:

Musts from Grillo autochthonous grapes grown in Western Sicily were fermented with medium toasted American oak wood chips or with non-toasted French oak chips. The obtained wines were significantly different in the contents in volatile and nonvolatile compounds extracted from the oak wood chips. Slight increases in alc. fermentation rate and in some cases higher contents of Et esters and medium-chain fatty acids were observed in musts fermented with the oak wood chips regardless of their origin. Wines made with French medium toasted oak wood chips had higher contents of phenolic aldehydes (syringic aldehyde, vanillin), furans (5-methylfurfural, trans-β-methyl-γ-octalactone), eugenol, tyrosol, and dihydromethoxycinnamyl alc. The wines made with oak wood chips had more complex sensory profiles and their aroma intensity was higher vs. control wines. Differences in visual and olfactory descriptors were also found. In the experiment, the researchers used many compounds, for example, Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0SDS of cas: 15399-05-0).

Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.SDS of cas: 15399-05-0

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

Liang, Zhanqun et al. published their research in Organic Chemistry Frontiers in 2021 | CAS: 13669-10-8

Ethyl 3-oxo-3-(thiophen-2-yl)propanoate (cas: 13669-10-8) 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. 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.Electric Literature of C9H10O3S

Visible-light photocatalytic preparation of alkenyl thioethers from 1,2,3-thiadiazoles and Hantzsch esters: synthetic and mechanistic investigations was written by Liang, Zhanqun;Lv, Kang;Zhou, Shaofang;Zhu, Changlei;Bao, Xiaoguang. And the article was included in Organic Chemistry Frontiers in 2021.Electric Literature of C9H10O3S This article mentions the following:

A protocol to synthesize trisubstituted alkenyl thioethers I (R1 = Ph, 3-ClC6H4, 2-naphthyl, 2-thienyl, etc.; R2 = i-Pr, cyclohexyl, PhCH2, PhCMe2, etc.) through a direct S-alkylation of 1,2,3-thiadiazoles II with C-radical precursors, 4-alkyl-1,4-dihydropyridines III (R3 = EtO2C, t-BuO2C, CN), driven by visible-light photocatalysis is disclosed. A broad range of primary, secondary and tertiary C-radical precursors is suitable for this reaction and the desired products can be obtained in good to excellent yields under mild conditions. Remarkably, high stereoselectivity with Z-alkenyl thioethers was achieved in the presence of a Cu(OAc)2 catalyst. Synergistic exptl. and computational studies were carried out to shed light on the mechanisms of this reaction, in which the quenching pathway of an excited photocatalyst (*RuII) could be altered in the presence of the Cu(OAc)2 catalyst. A reductive quenching pathway (RuII/*RuII/RuI/RuII) was proposed in the absence of the Cu(OAc)2 catalyst while an oxidative quenching pathway (RuII/*RuII/RuIII/RuII) was suggested with the assistance of the Cu(OAc)2 catalyst. In addition, the origin of the Z-selectivity of the product was discussed. In the experiment, the researchers used many compounds, for example, Ethyl 3-oxo-3-(thiophen-2-yl)propanoate (cas: 13669-10-8Electric Literature of C9H10O3S).

Ethyl 3-oxo-3-(thiophen-2-yl)propanoate (cas: 13669-10-8) 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. 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.Electric Literature of C9H10O3S

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

Trollsas, M. et al. published their research in Journal of Polymer Science, Part A: Polymer Chemistry in 1998 | CAS: 19444-23-6

Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) 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. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Quality Control of Benzyl 2-hydroxy-2-methylpropanoate

Internal functionalization in hyperbranched polyesters was written by Trollsas, M.;Hedrick, J.;Mecerreyes, D.;Jerome, R.;Dubois, Ph.. And the article was included in Journal of Polymer Science, Part A: Polymer Chemistry in 1998.Quality Control of Benzyl 2-hydroxy-2-methylpropanoate This article mentions the following:

Hyperbranched polyesters derived from the first and second generations of bis(hydroxymethyl)propionic acid (bis-MPA) benzyl esters to afford both AB2 and AB4 macromonomers, resp., were prepared The hyperbranched polyesters are effective initiators for the ROP of lactones, e.g., ε-caprolactone, in the presence of Sn(Oct)2. Even more complex mol. architectures were developed using 1,4,9-trioxaspiro[4.6]-9-undecanone (TOSUO) as comonomer, after sequential deacetalization and reduction steps. This procedure produces hyper-branched polymers with significant hydroxy functionality at the periphery of the macromol. as well as dispersed along the chain backbone. 199457-33-5P 199457-35-7P 199457-37-9P 199541-92-9P 199541-93-0P 199541-94-1. In the experiment, the researchers used many compounds, for example, Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6Quality Control of Benzyl 2-hydroxy-2-methylpropanoate).

Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) 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. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Quality Control of Benzyl 2-hydroxy-2-methylpropanoate

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

Wang, Baoyi et al. published their research in European Food Research and Technology in 2022 | CAS: 105-87-3

(E)-3,7-Dimethylocta-2,6-dien-1-yl acetate (cas: 105-87-3) 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. 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.Formula: C12H20O2

Identification of aroma-active components in black teas produced by six Chinese tea cultivars in high-latitude region by GC-MS and GC-O analysis was written by Wang, Baoyi;Chen, Huimin;Qu, Fengfeng;Song, Yakang;Di, Taimei;Wang, Peiqiang;Zhang, Xinfu. And the article was included in European Food Research and Technology in 2022.Formula: C12H20O2 This article mentions the following:

In this study, gas chromatog.-mass spectrometry (GC-MS) and gas chromatog.-olfactometry (GC-O) anal. was performed to figure out the characteristic aroma compounds of high-latitude black teas and select the suitable cultivar for producing high-aroma black tea. Sensory evaluation revealed that Jinxuan presented an obviously floral aroma and got the highest score, followed by Longjing Changye, Zhongcha 302, Yingshuang, Baihaozao and Huangshan Quntizhong. Furthermore, a total of 135 volatiles were identified in all black teas and 12 components can be used to distinguish different latitude black teas by principal component anal. (PCA). Cluster anal. (CA) showed six samples were divided into two clusters and Jinxuan was classified sep. of cluster B. Based on GC-O anal., 41 volatile organic compounds (VOCs) were found to promote the aroma of high-latitude black teas. Among them, phenylethyl alc., geraniol, linalool, α-ionone, cis-3-hexenyl hexanoate and Me salicylate were the major contributors to the floral fragrance of black tea and accounted for a relative high proportion in Jinxuan, Longjing Changye and Baihaozao. In summary, Jinxuan and Longjing Changye were suitable for producing high-quality black tea in high-latitude area. In the experiment, the researchers used many compounds, for example, (E)-3,7-Dimethylocta-2,6-dien-1-yl acetate (cas: 105-87-3Formula: C12H20O2).

(E)-3,7-Dimethylocta-2,6-dien-1-yl acetate (cas: 105-87-3) 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. 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.Formula: C12H20O2

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

Smith, Elizabeth M. et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2010 | CAS: 16413-26-6

3-Cyanophenylisocyanate (cas: 16413-26-6) 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. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Category: esters-buliding-blocks

T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones-optimization, design and synthesis was written by Smith, Elizabeth M.;Sorota, Steve;Kim, Hyunjin M.;McKittrick, Brian A.;Nechuta, Terry L.;Bennett, Chad;Knutson, Chad;Burnett, Duane A.;Kieselgof, Jane;Tan, Zheng;Rindgen, Diane;Bridal, Terry;Zhou, Xiaoping;Jia, Yu-Ping;Dong, Zoe;Mullins, Debbie;Zhang, Xiaoping;Priestley, Tony;Correll, Craig C.;Tulshian, Deen;Czarniecki, Michael;Greenlee, William J.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2010.Category: esters-buliding-blocks This article mentions the following:

A series of spiro-azetidines and azetidinones has been evaluated as novel blockers of the T-type calcium channel (CaV3.2) which is a new therapeutic target for the potential treatment of both inflammatory and neuropathic pain. Confirmation and optimization of the potency, selectivity and DMPK properties of leads will be described. In the experiment, the researchers used many compounds, for example, 3-Cyanophenylisocyanate (cas: 16413-26-6Category: esters-buliding-blocks).

3-Cyanophenylisocyanate (cas: 16413-26-6) 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. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Category: esters-buliding-blocks

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

Zhang, Yumeng et al. published their research in International Dairy Journal in 2021 | CAS: 706-14-9

5-Hexyldihydrofuran-2(3H)-one (cas: 706-14-9) 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. 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 C10H18O2

Effect of different heat treatments on the Maillard reaction products, volatile compounds and glycation level of milk was written by Zhang, Yumeng;Yi, Shengnan;Lu, Jing;Pang, Xiaoyang;Xu, Xiaoxi;Lv, Jiaping;Zhang, Shuwen. And the article was included in International Dairy Journal in 2021.Computed Properties of C10H18O2 This article mentions the following:

In this study, the formation of Maillard reaction products and the Maillard reaction sites of milk proteins were studied under different heat treatment conditions. Fifteen samples heated at 75, 90, 105, 120 or 135°C for 5, 15 or 30 s were selected to investigate the effects of different heat treatment conditions on the Maillard reaction products volatile compounds and protein glycation degree. The contents of fluorescence intensity, furosine, lactulose, and 5-hydroxymethylfural were pos. associated with the heat temperature and treatment time. Compared with that of raw milk, the number of glycated proteins increased from 14 to 49 in the milk samples heated at 135°C for 5 s, and the number of binding sites increased from 47 to 166. These results advance current knowledge about the effect of different heat treatments on the degree of the Maillard reaction and the sensory quality and glycation level of milk. In the experiment, the researchers used many compounds, for example, 5-Hexyldihydrofuran-2(3H)-one (cas: 706-14-9Computed Properties of C10H18O2).

5-Hexyldihydrofuran-2(3H)-one (cas: 706-14-9) 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. 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 C10H18O2

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