Category: 103-25-3

Recommanded Product: 103-25-3. In 2019.0 ACS SUSTAIN CHEM ENG published article about HETEROPOLY ACID; OXIDATIVE ESTERIFICATION; CARBON NITRIDE; FATTY-ACIDS; OLEIC-ACID; ALCOHOLS; NANOPARTICLES; DEHYDRATION; PERFORMANCE; ALDEHYDES in [Fiorio, Jhonatan Luiz; Braga, Adriano Henrique; Rossi, Liane Marcia] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, Av Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP, Brazil; [Fiorio, Jhonatan Luiz; Barbosa Guedes, Carmen Luisa] Univ Estadual Londrina, Dept Quim, Ctr Ciencias Exatas, BR-86057970 Londrina, PR, Brazil in 2019.0, Cited 69.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

Solid acid catalysts are environmentally friendly alternatives to the use of mineral acids in a range of applications, including the esterification of carboxylic acids. Here, a phosphorus- and nitrogen-doped, carbon-modified, fully heterogeneous solid acid catalyst was prepared by pyrolysis of a mixture of melamine and tungstophosphoric acid at 250, 500, and 750 degrees C under a nitrogen atmosphere provided. The structure of the different catalysts was evaluated by surface area measurements, XRD, XPS, Raman spectroscopy, elemental analysis, and electron microscopies. Pyrolysis at 500 degrees C created complex solid materials with larger surface area and significantly higher acidity, which can be attributed to WO3 formation on a heteroatomic (N,P)-carbon structure. The 500 degrees C-treated heterogeneous catalysts showed remarkably better activity for esterification of palmitic acid and were thus applied in the esterification of a broad range of carboxylic acids with good overall yields. Furthermore, the solid acid catalyst can be easily recovered and recycled up to eight times without significant loss of activity with no leaching of species to the reaction mixture.

Recommanded Product: 103-25-3. About Methyl 3-phenylpropionate, If you have any questions, you can contact Fiorio, JL; Braga, AH; Guedes, CLB; Rossi, LM or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Category: esters-buliding-blocks. Recently I am researching about CATALYZED TRANSFER HYDROGENATION; STEREOSELECTIVE TRANSFER SEMIHYDROGENATION; HIGHLY-ACTIVE HYDROGENATION; ORGANIC FRAMEWORK NODES; SITE COBALT CATALYSTS; BORANE-AMINE ADDUCTS; SELECTIVE HYDROGENATION; CONJUGATE REDUCTION; AMMONIA-BORANE; ASYMMETRIC HYDROGENATION, Saw an article supported by the Ministry of Science and Technology of ChinaMinistry of Science and Technology, China [2016YFE0132600]; Henan Center for Outstanding Overseas Scientists [GZS2020001]; National Innovation and Entrepreneurship Training Program for College students [201910459064]; Zhengzhou University. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Wang, Y; Cao, XY; Zhao, LY; Pi, C; Ji, JF; Cui, XL; Wu, YJ. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

A generalized, simple and efficient transfer hydrogenation of unsaturated bonds has been developed using HBP in and various proton reagents as hydrogen sources. The substrates, including alkenes, alkynes, aromatic heterocycles, aldehydes, ketones, imines, azo, nitro, epoxy and nitrile compounds, are all applied to this catalytic system. Various groups, which cannot survive under the Pd/C/H-2 combination, are tolerated. The activity of the reactants was studied and the trends are as follows:styrene>diphenylmethanimine>benzaldehyde>azobenzene>nitrobenzene>quinoline>acetophenone>benzonitrile. Substrates bearing two or more different unsaturated bonds were also investigated and transfer hydrogenation occurred with excellent chemoselectivity. Nano-palladium catalystin situgenerated from Pd(OAc)(2) and HBP in extremely improved the TH efficiency. Furthermore, chemoselective anti-Markovnikov hydrodeuteration of terminal aromatic olefins was achieved using D2O and HBP in via in situ HD generation and discrimination.

Category: esters-buliding-blocks. About Methyl 3-phenylpropionate, If you have any questions, you can contact Wang, Y; Cao, XY; Zhao, LY; Pi, C; Ji, JF; Cui, XL; Wu, YJ or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Cobalt-catalyzed direct transformation of aldehydes to esters: the crucial role of an enone as a mediator WOS:000462670600012 published article about CHEMOSELECTIVE TRANSFER HYDROGENATION; C-H FUNCTIONALIZATION; OXIDATIVE ESTERIFICATION; TISHCHENKO REACTIONS; PRIMARY ALCOHOLS; INTERMOLECULAR HYDROACYLATION; INTRAMOLECULAR HYDROACYLATION; ALDOL CONDENSATIONS; BENZYLIC ALCOHOLS; COMPLEXES in [Jiang, Biao-Lin; Wang, Meng-Liang; Liu, Dian-Sheng] Shanxi Univ, Sch Chem & Chem Engn, Taiyuan 030006, Shanxi, Peoples R China; [Jiang, Biao-Lin; Lin, Yang; Xu, Bao-Hua; Zhang, Suo-Jiang] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing Key Lab Ion Liquids Clean Proc,Key Lab Gr, Beijing 100190, Peoples R China; [Lin, Yang] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China in 2019.0, Cited 73.0. Product Details of 103-25-3. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

An oxidative esterification of aldehydes with alkanols catalyzed by an in situ generated low-valent cobalt system has been developed using an enone as a mild oxidant. Mechanistic studies revealed that it proceeds through a Co(i)-catalyzed hydrogen-transfer route, wherein the -vinyl moiety in the bidentate enone functions as a hydride acceptor. Meanwhile, Co(i)-catalyzed formyl C-H activation occurred as a competing reaction leading to aldehyde dimerization. The occurrence of the usually kinetically disfavored hydride transfer step therein was significantly increased in the presence of an enone reacting as a hydride transfer initiator.

About Methyl 3-phenylpropionate, If you have any questions, you can contact Jiang, BL; Lin, Y; Wang, ML; Liu, DS; Xu, BH; Zhang, SJ or concate me.. Product Details of 103-25-3

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Recently I am researching about OILS; SESQUITERPENOIDS; CONSTITUENTS; MALAYSIA, Saw an article supported by the National Science Foundation for Young Scientists of China [21904120]. Application In Synthesis of Methyl 3-phenylpropionate. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Sun, YA; Zhang, HM; Li, ZX; Yu, WH; Zhao, ZJ; Wang, K; Zhang, ML; Wang, JT. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

Agarwood, a species of resinous heartwood, is a precious medicinal plant and a type of rare natural spice, which is widely used in medicine, cosmetics, religious activities, and other fields. In this study, agarwood samples from eight different regions across four countries were analyzed by comprehensive two-dimensional gas chromatography-quadrupole time-of-flight mass spectrometry. A total of 232 species were identified (the match factors of these compounds were above 750). The main compounds of agarwood are oxygenated sesquiterpenes and chromones. The compositions of India1 and Malaysia2 were significantly different from those of other samples, which might be attributed to the different production processes of agarwood. For further investigation, factor analysis was conducted for six agarwood samples. The results showed that the data classification possessed a regional characteristic; according to the retention time and relative content, characteristic compositions were determined by factor scores. Finally, the differences of characteristic compositions were simply analyzed, and the reasons were speculated.

Application In Synthesis of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Sun, YA; Zhang, HM; Li, ZX; Yu, WH; Zhao, ZJ; Wang, K; Zhang, ML; Wang, JT or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Recently I am researching about BETA-CARYOPHYLLENE; ANTIOXIDANT ACTIVITY; ANTIMICROBIAL ACTIVITY; CYTOTOXIC ACTIVITIES; BIOACTIVE COMPOUNDS; RED PROPOLIS; BEE POLLEN; D-LIMONENE; FT-IR; ORIGIN, Saw an article supported by the Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil vide research Project on Instituto Nacional de Ciencia e Tecnologia de Frutos TropicaisConselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPQ) [57573781/2008-7]. Published in ELSEVIER in AMSTERDAM ,Authors: Olegario, LS; Andrade, JKS; Andrade, GRS; Denadai, M; Cavalcanti, RL; da Silva, MAAP; Narain, N. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate. Formula: C10H12O2

The aim of this work was to undertake a detailed analysis on chemical constituents of brown propolis, originating from four different states (Bahia, Minas Gerais, Parana and Sergipe) of Brazil. The volatile profile was determined by using HS-SPME-GC-MS along with the determination of total phenolic compounds content, flavonoids and antioxidant activity. A total of 315 volatile compounds were identified, however, several of them have not been reported so far in the Brazilian brown propolis. The terpenes represented the major class with 40.92-84.66% of the total area in the chromatograms. PCA analysis of the majority of compounds successfully indicated the volatile profile of each propolis sample according to their geographical origin. The analysis of volatile compounds and its characterization also varied significantly and confirmed that these depended on the geographical area of collection of propolis. The data generated in this work may help in establishing criteria for quality control and tracking the specific region of propolis production in different states of Brazil.

Formula: C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Olegario, LS; Andrade, JKS; Andrade, GRS; Denadai, M; Cavalcanti, RL; da Silva, MAAP; Narain, N or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Li, XJ; Ding, J; Li, N; Liu, WX; Ding, FH; Zheng, HJ; Ning, YY; Wang, HM; Liu, RM; Ren, SD in [Li, Xiaojing; Li, Ning; Liu, Wenxia; Ding, Fuhao; Zheng, Huijuan; Ning, Yanyan; Wang, Hongmin; Liu, Renmin] Liaocheng Univ, Sch Pharm, Liaocheng 252000, Shandong, Peoples R China; [Ding, Jie; Ren, Shaoda] Liaocheng Peoples Hosp, Cent Lab, Liaocheng 252000, Shandong, Peoples R China published Synthesis and biological evaluation of celastrol derivatives as anti-ovarian cancer stem cell agents in 2019.0, Cited 31.0. Category: esters-buliding-blocks. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

Ovarian cancer is associated with a high percentage of recurrence of tumors and resistance to chemotherapy. Cancer stem cells (CSCs) are responsible for cancer progression, tumor recurrence, metastasis, and chemoresistance. Thus, developing CSC-targeting therapy is an urgent need in cancer research and clinical application. In an attempt to achieve potent and selective anti-CSC agents, a series of celastrol derivatives with cinnamamide chains were synthesized and evaluated for their anti-ovarian cancer activities. Most of the compounds exhibited stronger antiproliferative activity than celastrol, and celastrol derivative 7g with a 3,4,5-trimethoxycinnamamide side chain was found to be the most potent antiproliferative agent against ovarian cancer cells with an IC50 value of 0.6 mu M. Additionally, compound 7g significantly inhibited the colony formation ability and reduced the number of tumor spheres. Furthermore, compound 7g decreased the percentage of CD44(+), CD133(+) and ALDH(+) cells. Thus, compound 7g is a promising anti-CSC agent and could serve as a candidate for the development of new antiovarian cancer drugs. (C) 2019 Elsevier Masson SAS. All rights reserved.

Category: esters-buliding-blocks. About Methyl 3-phenylpropionate, If you have any questions, you can contact Li, XJ; Ding, J; Li, N; Liu, WX; Ding, FH; Zheng, HJ; Ning, YY; Wang, HM; Liu, RM; Ren, SD or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Synthesis and biological evaluation of celastrol derivatives as anti-ovarian cancer stem cell agents WOS:000486133100049 published article about DESIGN in [Li, Xiaojing; Li, Ning; Liu, Wenxia; Ding, Fuhao; Zheng, Huijuan; Ning, Yanyan; Wang, Hongmin; Liu, Renmin] Liaocheng Univ, Sch Pharm, Liaocheng 252000, Shandong, Peoples R China; [Ding, Jie; Ren, Shaoda] Liaocheng Peoples Hosp, Cent Lab, Liaocheng 252000, Shandong, Peoples R China in 2019.0, Cited 31.0. HPLC of Formula: C10H12O2. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

Ovarian cancer is associated with a high percentage of recurrence of tumors and resistance to chemotherapy. Cancer stem cells (CSCs) are responsible for cancer progression, tumor recurrence, metastasis, and chemoresistance. Thus, developing CSC-targeting therapy is an urgent need in cancer research and clinical application. In an attempt to achieve potent and selective anti-CSC agents, a series of celastrol derivatives with cinnamamide chains were synthesized and evaluated for their anti-ovarian cancer activities. Most of the compounds exhibited stronger antiproliferative activity than celastrol, and celastrol derivative 7g with a 3,4,5-trimethoxycinnamamide side chain was found to be the most potent antiproliferative agent against ovarian cancer cells with an IC50 value of 0.6 mu M. Additionally, compound 7g significantly inhibited the colony formation ability and reduced the number of tumor spheres. Furthermore, compound 7g decreased the percentage of CD44(+), CD133(+) and ALDH(+) cells. Thus, compound 7g is a promising anti-CSC agent and could serve as a candidate for the development of new antiovarian cancer drugs. (C) 2019 Elsevier Masson SAS. All rights reserved.

HPLC of Formula: C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Li, XJ; Ding, J; Li, N; Liu, WX; Ding, FH; Zheng, HJ; Ning, YY; Wang, HM; Liu, RM; Ren, SD or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Recently I am researching about CARBON-CARBON BONDS; ARYL KETONES; ACTIVATION; EXCHANGE, Saw an article supported by the Education Department of Shaanxi Provincial Government [2018JM2012]; Shaanxi Provincial Education Department [17JS129, 17JK0773]; Key Science and Technology Innovation Team of Shaanxi Province [2017KCT-37]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Jiang, C; Wu, WQ; Lu, H; Yu, TY; Xu, WH; Wei, H. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate. SDS of cas: 103-25-3

A Rh-III-catalyzed Hiyama cross-coupling reaction has been successfully developed. Cleavage of the less polar C-C bond provides an efficient strategy to enable ketones to be as electrophilic reagents, and the corresponding substituted indoles with diverse functional groups are efficiently synthesized in good to high yields.

SDS of cas: 103-25-3. About Methyl 3-phenylpropionate, If you have any questions, you can contact Jiang, C; Wu, WQ; Lu, H; Yu, TY; Xu, WH; Wei, H or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Pd-catalyzed alkoxycarbonylation of alkenes promoted by H2O free of auxiliary acid additive WOS:000514756200040 published article about PALLADIUM COMPLEXES; DIRECT CARBONYLATION; METHOXYCARBONYLATION; LIGANDS; HYDROESTERIFICATION; STYRENE; EFFICIENT; DIPHOSPHINES; MECHANISM; OLEFINS in [Liang, Wen-Yu; Liu, Lei; Zhou, Qing; Yang, Da; Lu, Yong; Liu, Ye] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, 3663 North Zhongshan Rd, Shanghai 200062, Peoples R China in 2020.0, Cited 33.0. Application In Synthesis of Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

The Pd-catalyzed alkoxycarbonylation of alkenes using water as a promoter has been scarcely reported before. Herein, water instead of Bronsted/Lewis acid was found to effectively improve the catalytic performance of Pd (MeCN)(2)Cl-2-Xantphos system for alkoxycarbonylation of alkenes. Under the optimal conditions, the best yield of 97% was obtained for the target products (methyl 3-phenylpropanoate and methyl 2-phenylpropanoate) with L/B of 4.3 and TON of 192. With the involvement of water, Pd(MeCN)(2)Cl-2-Xantphos system also exhibited the moderate to good generality to alkoxycarbonylation of different kinds of alkenes with alcohols. The in situ high pressure FT-IR analysis verified that water played an important role in promoting formation and stability of Pd-H active species which was responsible for the efficient alkoxycarbonylation of alkenes. In addition, the ligand effect of Xantphos on this reaction was discussed.

About Methyl 3-phenylpropionate, If you have any questions, you can contact Liang, WY; Liu, L; Zhou, Q; Yang, D; Lu, Y; Liu, Y or concate me.. Application In Synthesis of Methyl 3-phenylpropionate

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Computed Properties of C10H12O2. Recently I am researching about TRIAZINES; AMINES, Saw an article supported by the JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [26293003, 17H03970, 19K06994]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Kitamura, M; Komine, S; Yamada, K; Kunishima, M. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

Herein, we report on the synthesis of alkyl-, aryl-, and alkynyl-substituted chlorotriazines and their ammonium salts, and demonstrate their utility in dehydrative condensation reactions. Although the electrophilicity of these reagents is mainly dependent on the hybridization of the carbon-substituents, it was found that bulky 2,6-dimethylphenyl group-substituted reagents resulted in the highest product yields because of a slight increase in reagent electrophilicity and/or steric hindrance favorable for desired dehydrative condensation reactions. (C) 2019 Elsevier Ltd. All rights reserved.

Computed Properties of C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Kitamura, M; Komine, S; Yamada, K; Kunishima, M or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics