Qiu, Li et al. published their research in Journal of Organic Chemistry in 2014 | CAS: 14667-47-1

Methyl 2-aminonicotinate (cas: 14667-47-1) 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 contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C 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. Application of 14667-47-1

Reductive Ring Closure Methodology toward Heteroacenes Bearing a Dihydropyrrolo[3,2-b]pyrrole Core: Scope and Limitation was written by Qiu, Li;Wang, Xiao;Zhao, Na;Xu, Shiliang;An, Zengjian;Zhuang, Xuhui;Lan, Zhenggang;Wen, Lirong;Wan, Xiaobo. And the article was included in Journal of Organic Chemistry in 2014.Application of 14667-47-1 This article mentions the following:

A newly developed reductive ring closure methodol. to heteroacenes bearing a dihydropyrrolo[3,2-b]pyrrole core, e.g., I (R = n-octyl), was systematically studied for its scope and limitation. The methodol. involves (i) the cyclization of an o-aminobenzoic acid ester derivative to give an eight-membered cyclic dilactam, and (ii) the conversion of the dilactams into the corresponding diimidoyl chloride, which undergoes (iii) reductive ring closure to install the dihydropyrrolo[3,2-b]pyrrole core. The first step of the methodol. plays the key role due to its substrate limitation, which suffers from the competition of oligomerization and hydrolysis. All the dilactams could successfully convert to the corresponding diimidoyl chlorides, most of which succeeded to give the dihydropyrrolo[3,2-b]pyrrole core. The influence of the substituents and the elongation of conjugated length on the photophys. properties of the obtained heteroacenes were then investigated systematically using UV-vis spectroscopy and cyclic voltammetry. It was found that chlorination and fluorination had quite a different effect on the photophys. properties of the heteroacene, and the ring fusing pattern also had a drastic influence on the band gap of the heteroacene. The successful preparation of a series of heteroacenes bearing a dihydropyrrolo[3,2-b]pyrrole core would provide a wide variety of candidates for further fabrication of organic field-effect transistor devices. In the experiment, the researchers used many compounds, for example, Methyl 2-aminonicotinate (cas: 14667-47-1Application of 14667-47-1).

Methyl 2-aminonicotinate (cas: 14667-47-1) 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 contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C 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. Application of 14667-47-1

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

Zhang, Dan et al. published their research in Huaxue Shiji in 2014 | CAS: 106-79-6

Dimethyl decanedioate (cas: 106-79-6) 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. 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.Recommanded Product: Dimethyl decanedioate

Transesterification of ethylene carbonate with dimethyl sebacate was written by Zhang, Dan;Li, Jun-hua. And the article was included in Huaxue Shiji in 2014.Recommanded Product: Dimethyl decanedioate This article mentions the following:

The transesterification of ethylene carbonate (EC) and di-Me sebacate (DMS) was investigated over metal acetate catalysts. The main product was proved to be di-Me carbonate (DMC) by GC-MS, which was an environmentally benign chem. intermediate. At the same time, a new kind of aliphatic polyester could be synthesized, which could be biodegraded. This method improved the atom economy, avoiding the formation of byproduct methanol and ethylene glycol and made good use of CO2. The results showed Li(CH3COO)·2H2O had the highest activity. Effects of reaction temperature, catalyst amount, ratio of reactant and reaction time on yields of di-Me carbonate was investigated. When the reaction was carried out 250°C, with mole ratio catalyst to DMS of 0.004, mole ratio of EC to DMS of 3:1, reaction time 3 h, the yield of DMC was 45.7%. In the experiment, the researchers used many compounds, for example, Dimethyl decanedioate (cas: 106-79-6Recommanded Product: Dimethyl decanedioate).

Dimethyl decanedioate (cas: 106-79-6) 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. 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.Recommanded Product: Dimethyl decanedioate

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

Schiebel, Johannes et al. published their research in ACS Chemical Biology in 2016 | CAS: 41191-92-8

Ethyl 3-amino-4-methylbenzoate (cas: 41191-92-8) 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.COA of Formula: C10H13NO2

Six Biophysical Screening Methods Miss a Large Proportion of Crystallographically Discovered Fragment Hits: A Case Study was written by Schiebel, Johannes;Radeva, Nedyalka;Krimmer, Stefan G.;Wang, Xiaojie;Stieler, Martin;Ehrmann, Frederik R.;Fu, Kan;Metz, Alexander;Huschmann, Franziska U.;Weiss, Manfred S.;Mueller, Uwe;Heine, Andreas;Klebe, Gerhard. And the article was included in ACS Chemical Biology in 2016.COA of Formula: C10H13NO2 This article mentions the following:

Fragment-based lead discovery (FBLD) has become a pillar in drug development. Typical applications of this method comprise at least two biophys. screens as prefilter and a follow-up crystallog. experiment on a subset of fragments. Clearly, structural information is pivotal in FBLD, but a key question is whether such a screening cascade strategy will retrieve the majority of fragment-bound structures. We therefore set out to screen 361 fragments for binding to endothiapepsin, a representative of the challenging group of aspartic proteases, employing six screening techniques and crystallog. in parallel. Crystallog. resulted in the very high number of 71 structures. Yet alarmingly, 44% of these hits were not detected by any biophys. screening approach. Moreover, any screening cascade, building on the results from two or more screening methods, would have failed to predict at least 73% of these hits. We thus conclude that, at least in the present case, the frequently applied biophys. prescreening filters deteriorate the number of possible X-ray hits while only the immediate use of crystallog. enables exhaustive retrieval of a maximum of fragment structures, which represent a rich source guiding hit-to-lead-to-drug evolution. In the experiment, the researchers used many compounds, for example, Ethyl 3-amino-4-methylbenzoate (cas: 41191-92-8COA of Formula: C10H13NO2).

Ethyl 3-amino-4-methylbenzoate (cas: 41191-92-8) 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.COA of Formula: C10H13NO2

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

Lamande-Langle, Sandrine et al. published their research in Chemical Communications (Cambridge, United Kingdom) in 2010 | CAS: 17920-23-9

Diethyl 2-(prop-2-yn-1-yl)malonate (cas: 17920-23-9) 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.Name: Diethyl 2-(prop-2-yn-1-yl)malonate

Domino allylic amination/Sonogashira/heterocyclisation reactions: palladium-catalysed three-component synthesis of pyrroles was written by Lamande-Langle, Sandrine;Abarbri, Mohamed;Thibonnet, Jerome;Duchene, Alain;Parrain, Jean-Luc. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2010.Name: Diethyl 2-(prop-2-yn-1-yl)malonate This article mentions the following:

Three-component reactions with 3,4-diiodoalk-2-enoic derivatives, primary amines, and terminal alkynes proceeded to give trisubstituted pyrroles, e.g., I in fair to good yields in the presence of palladium and copper catalysts under mild reaction conditions. In the experiment, the researchers used many compounds, for example, Diethyl 2-(prop-2-yn-1-yl)malonate (cas: 17920-23-9Name: Diethyl 2-(prop-2-yn-1-yl)malonate).

Diethyl 2-(prop-2-yn-1-yl)malonate (cas: 17920-23-9) 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.Name: Diethyl 2-(prop-2-yn-1-yl)malonate

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

Yang, Jian et al. published their research in Chemical Science in 2019 | CAS: 584-74-7

Ethyl 2-fluorophenylacetate (cas: 584-74-7) 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. 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.Electric Literature of C10H11FO2

Enantioselective carbene insertion into the N-H bond of benzophenone imine was written by Yang, Jian;Ruan, Peiran;Yang, Wei;Feng, Xiaoming;Liu, Xiaohua. And the article was included in Chemical Science in 2019.Electric Literature of C10H11FO2 This article mentions the following:

Efficient enantioselective insertion of α-diazoesters into the N-H bond of N-sp2-hybridized benzophenone imine was realized by using Rh2(esp)2 and chiral guanidine cooperative catalysis. Both aliphatic and aromatic substituted α-amino esters were obtained in high yields (up to 99%) and good enantioselectivities (up to 95.5 : 4.5 er) under mild reaction conditions. In the experiment, the researchers used many compounds, for example, Ethyl 2-fluorophenylacetate (cas: 584-74-7Electric Literature of C10H11FO2).

Ethyl 2-fluorophenylacetate (cas: 584-74-7) 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. 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.Electric Literature of C10H11FO2

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

Gurkan, H. et al. published their research in Journal of Food Safety in 2018 | CAS: 659-70-1

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. 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.Related Products of 659-70-1

Volatile compounds and biogenic amines during the ripening of mold-ripened Civil cheese manufactured using three different strains of Penicillium roqueforti was written by Gurkan, H.;Yilmaztekin, M.;Cakmakci, S.;Hayaloglu, A. A.. And the article was included in Journal of Food Safety in 2018.Related Products of 659-70-1 This article mentions the following:

Three different strains of Penicillium roqueforti were used for the manufacture of mold-ripened Civil cheese and these cheeses were ripened at 4 and 10 °C for 90 days. Sixty-five volatile compounds were identified in the volatile fractions of the cheeses. The concentration of volatile compounds in cheeses was significantly affected ripening time temperature and by mold strains a lesser extent. 3-Methyl-1-butanol, 2-nonanol, Me dodecanoate, butanoic acid, and decanoic acid were the most frequently identified volatiles. Tryptamine, 2-phenylethylamine, putrescine, cadaverine, tyramine, spermidine, and spermine were also found. The most abundant biogenic amine was cadaverine. The formation of biogenic amines was significantly influenced by strain, ripening time, and temperature The biogenic amine content was found to be between 2.41 and 228.94 μg/g cheese. Ripening temperature and ripening time significantly influenced the formation of volatile compounds and biogenic amines. Practical applications : Moldy Civil is a traditional cheese variety produced in the eastern Anatolian region of Turkey and it is protected by geog. indication by Turkish Patent and Trademark Office (TURKPATENT) by 2010. It is manufactured using skimmed milk which is spontaneously acidified with native lactic acid bacteria and also the addition of preacidified whey. Three strains of P. roqueforti was used in Moldy Civil cheese-making and strains of the mold changed the volatile profiles and the levels of biogenic amines less than ripening time and temperature Me ketones and alcs. were the dominant groups in volatiles, while cadaverine was found to be principal biogenic amine in Moldy Civil cheese. Use of P. roqueforti strains contributed to the formation of the volatile fraction of the cheese; however, the level of biogenic amines changed by P. roqueforti strains a lesser extent. In the experiment, the researchers used many compounds, for example, Isopentyl 3-methylbutanoate (cas: 659-70-1Related Products of 659-70-1).

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. 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.Related Products of 659-70-1

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

Wang, Yan et al. published their research in Environmental Pollution (Oxford, United Kingdom) in 2021 | CAS: 84-61-7

Dicyclohexyl phthalate (cas: 84-61-7) 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. 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.Computed Properties of C20H26O4

Characteristics and risk assessment of organophosphate esters and phthalates in soils and vegetation from Dalian, northeast China was written by Wang, Yan;Zhang, Zihao;Bao, Meijun;Xu, Yue;Zhang, Lijie;Tan, Feng;Zhao, Hongxia. And the article was included in Environmental Pollution (Oxford, United Kingdom) in 2021.Computed Properties of C20H26O4 This article mentions the following:

We investigated the concentration, composition, and potential risk of organophosphate esters (OPEs) and phthalates (PAEs) in soils and vegetation from rural areas of Dalian, Northeast China. The residues of total OPEs and PAEs in soils were in the range of 33.1-136 ng/g dw (dry weight) and 465-5450 ng/g dw, while the values in plants were 140-2360 ng/g dw and 2440-21800 ng/g dw, resp. The concentrations of both chems. in the plant rhizosphere soils were significantly lower than those in the bulk soils, suggesting an enhanced degradation or uptake by plant. The contaminations in soils also varied for different land use types with the concentrations generally higher in paddy soils than those in maize soils. The OPE and PAE concentrations in plant leaves were slightly higher than those in their corresponding roots. The bioconcentration factors of OPEs & PAEs were significantly neg. correlated with their octanol-water partition coefficients A hazard assessment suggested potential medium to high risks from tricresyl phosphate (TMPP) and di-Bu phthalate (DNBP) for the agricultural soils in Dalian of China. Although the ecol. risks of OPEs and PAEs in the rhizosphere soils were lower than those in the bulk soils, the relevant risk could still endanger human health via oral intake of these plants. The daily dietary intakes of OPEs and PAEs via vegetable and rice consuming were estimated, and the result suggests a higher exposure risk via ingestion of leafy vegetable than rice. In the experiment, the researchers used many compounds, for example, Dicyclohexyl phthalate (cas: 84-61-7Computed Properties of C20H26O4).

Dicyclohexyl phthalate (cas: 84-61-7) 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. 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.Computed Properties of C20H26O4

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

Rota, Paola et al. published their research in Angewandte Chemie, International Edition in 2010 | CAS: 6730-10-5

(2S,3S,4R,5S,6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate (cas: 6730-10-5) 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. 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.HPLC of Formula: 6730-10-5

General and Chemoselective N-Transacylation of Secondary Amides by Means of Perfluorinated Anhydrides was written by Rota, Paola;Allevi, Pietro;Colombo, Raffaele;Costa, Maria L.;Anastasia, Mario. And the article was included in Angewandte Chemie, International Edition in 2010.HPLC of Formula: 6730-10-5 This article mentions the following:

The utility of chemoselective N-transacylation of secondary amides has a broad scope in synthetic chem. Secondly, the two-step replacement of acyl groups of secondary amides with a different on through the formation of a trifluoro intermediate allows one to prepare simple acyl analogs of a variety of pharmaceutical interest. Further, this reaction is useful in anal. protocols where N-transacylation can be overlooked due to puzzling results. In the experiment, the researchers used many compounds, for example, (2S,3S,4R,5S,6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate (cas: 6730-10-5HPLC of Formula: 6730-10-5).

(2S,3S,4R,5S,6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate (cas: 6730-10-5) 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. 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.HPLC of Formula: 6730-10-5

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

Wang, Songmeng et al. published their research in ACS Applied Polymer Materials in 2020 | CAS: 27249-90-7

Benzyl benzodithioate (cas: 27249-90-7) 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. 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.Product Details of 27249-90-7

Multiple Stimuli-Responsiveness Fluorescent Probe Derived from Cyclopolymers and Pyrene-Ended Ammonium Salts was written by Wang, Songmeng;Yang, Yi;Shi, Xiaoyu;Liu, Lingyan;Chang, Weixing;Li, Jing. And the article was included in ACS Applied Polymer Materials in 2020.Product Details of 27249-90-7 This article mentions the following:

A multiple stimuli-responsiveness fluorescent probe was fabricated by host-guest recognition between cyclopolymers with larger pseudo crown ether cavities in backbones and pyrene-ended ammonium salts. And this fluorescent probe exhibits ratiometric responsiveness to chloride anion, organic base, and temperature, as well as a dual luminescence responsiveness to nitro-compounds These properties of this probe endow it with potential application in multiple stimuli-responsive chem. fluorescent sensors. Moreover, it was found that the cyclopolymers with pyrenes grafted on the backbone increased excimer/monomer emission ratio of the fluorescent polypseudorotaxane, which would be expected to present higher sensitivity and responsiveness to external environment or stimuli-factors. In the experiment, the researchers used many compounds, for example, Benzyl benzodithioate (cas: 27249-90-7Product Details of 27249-90-7).

Benzyl benzodithioate (cas: 27249-90-7) 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. 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.Product Details of 27249-90-7

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

Lovins, R. E. et al. published their research in Journal of Organic Chemistry in 1965 | CAS: 81245-24-1

Methyl 2-methoxy-4-methylbenzoate (cas: 81245-24-1) 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.Computed Properties of C10H12O3

The competitive rates of reaction of a series of substituted benzyl methyl ethers with N-bromosuccinimide was written by Lovins, R. E.;Andrews, L. J.;Keefer, R. M.. And the article was included in Journal of Organic Chemistry in 1965.Computed Properties of C10H12O3 This article mentions the following:

The relative rates of reaction of a series of nuclear-substituted benzyl methyl ethers (XC6H4CH2OCH3) with N-bromosuccinimide in carbon tetrachloride are not highly sensitive to the influence of ring substituents. The small variations in substituent effects observed for the reaction do not parallel those expected for a transition state involving development of negative charge on the benzylic carbon but rather favor a transition state involving positive polarization of the reaction center. On the basis of the substituent effects observed in the reaction of benzyl methyl ethers with N-bromosuccinimide and the results of a determination of the relative rates of reaction of p-nitro- and p-methoxyethylbenzene (XC6H4CH2CH3) and of p-methoxybenzyl cyanide (p-CH3OC6H4CH2CN) with N-bromosuccinimide, it has been concluded that the magnitude of the effect of a ring substituent X on the benzyl hydrogen abstraction process is controlled primarily by the ability of the group Y to contribute to the intrinsic stability of the radical (XC6H4CHY) being formed in the activation process. In the experiment, the researchers used many compounds, for example, Methyl 2-methoxy-4-methylbenzoate (cas: 81245-24-1Computed Properties of C10H12O3).

Methyl 2-methoxy-4-methylbenzoate (cas: 81245-24-1) 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.Computed Properties of C10H12O3

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