Machine Learning in Chemistry about Methyl 3-phenyl-2-propenoate

Recommanded Product: 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Zhou, CQ; Li, CZ; Siva, S; Cui, HY; Lin, L or concate me.

Authors Zhou, CQ; Li, CZ; Siva, S; Cui, HY; Lin, L in ELSEVIER published article about ESCHERICHIA-COLI O157H7; B-DNA DODECAMER; STAPHYLOCOCCUS-AUREUS; ANTIMICROBIAL ACTIVITY; ANTIOXIDANT ACTIVITY; BINDING; FOOD; STRAINS; DOCKING; MODE in [Zhou, Changqian; Siva, Subramanian; Cui, Haiying; Lin, Lin] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang 212013, Jiangsu, Peoples R China; [Li, Changzhu; Lin, Lin] Hunan Acad Forestry, State Key Lab Utilizat Woody Oil Resource, Changsha 410007, Peoples R China in 2021.0, Cited 76.0. Recommanded Product: 103-26-4. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

In this research, the antibacterial activity and the interaction mechanisms of the major chemical constituent present in the Alpinia galanga rhizomes essential oil (AGREO) were investigated. Ethyl cinnamate, methyl cinnamate and n-pentadecane were the major components of AGREO. The antibacterial mechanism of AGREO on Enterohemorrhagic Escherichia coli O157:H7 (EHEC O157) was evaluated and the results proved that the potent antibacterial activity of AGREO was due to higher passive permeability of bacterial cell membrane, followed by crucial intracellular components efflux. Additionally, AGREO disrupted the intracellular physiological metabolism of EHEC O157, including inhibition of P-type ATPases activity and down-regulation expression of four virulence genes associated with EHEC infections. Notably, molecular docking studies suggested that ethyl cinnamate probably competed with the structural NAD(P)(+) for the binding sites of glucose-6-phosphate dehydrogenase (G6PD), resulting in a decrease in G6PD activity with subsequent suppression of respiratory metabolism. The spectroscopic techniques and molecular docking studies proved that the AGREO major components were prone to bind to the minor groove of DNA.

Recommanded Product: 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Zhou, CQ; Li, CZ; Siva, S; Cui, HY; Lin, L or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
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Extracurricular laboratory: Synthetic route of Methyl 3-phenyl-2-propenoate

COA of Formula: C10H10O2. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Jiang, TY; Yuan, Y; Liu, SJ; Hunt, AJ; Tan, G or concate me.

Recently I am researching about CROSS-COUPLING REACTION; MESOPOROUS SILICA; PD NANOPARTICLES; HECK REACTIONS; MIZOROKI-HECK; PYROLYSIS; CATALYST; SOLVENT; REACTOR; SUZUKI, Saw an article supported by the . COA of Formula: C10H10O2. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Jiang, TY; Yuan, Y; Liu, SJ; Hunt, AJ; Tan, G. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

A highly active and recyclable Pd-deposited catalyst has been successfully prepared for the Heck reaction. Bio-oil liquid, a byproduct from the microwave pyrolysis of wastepaper, is employed to immobilize palladium nanoparticles on a solid support. FTIR, GC, and NMR results indicate the self-polymerization feature of bio-oil, thus giving rise to a uniform carbonaceous layer coated around the surface of the catalyst. Characteristic analysis of the catalyst indicates that palladium nanoparticles are well-dispersed on the parent SBA-15 solid substrate, which is attributed to the carbonaceous layer that is derived from bio-oil carbonization, allowing a high catalytic performance as a heterogeneous catalyst for the Heck reaction. The as-synthesized catalyst demonstrates remarkable recyclability with firm deposition of palladium nanoparticles on the solid support and could be reused without a activity. dramatic decrease in catalytic activity.

COA of Formula: C10H10O2. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Jiang, TY; Yuan, Y; Liu, SJ; Hunt, AJ; Tan, G or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Chemical Properties and Facts of 103-26-4

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Cheung, CW; Shen, N; Wang, SP; Ullah, A; Hu, XL; Ma, JA or concate me.. Application In Synthesis of Methyl 3-phenyl-2-propenoate

Application In Synthesis of Methyl 3-phenyl-2-propenoate. In 2019 ORG CHEM FRONT published article about AMIDE BOND FORMATION; PEPTIDE COUPLING REAGENTS; SECONDARY AMIDES; CARBOXYLIC-ACIDS; TRANSAMIDATION; METAL; HYDROAMINATION; ACTIVATION; AMINES in [Cheung, Chi Wai; Shen, Ni; Wang, Shao-Peng; Ullah, Asim; Ma, Jun-An] Tianjin Univ, Dept Chem, Tianjin Key Lab Mol Optoelect Sci, Tianjin 300072, Peoples R China; [Cheung, Chi Wai; Shen, Ni; Wang, Shao-Peng; Ullah, Asim; Ma, Jun-An] Tianjin Univ, Tianjin Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China; [Hu, Xile] Ecole Polytech Fed Lausanne, ISIC LSCI, Inst Chem Sci & Engn, Lab Inorgan Synth & Catalysis, BCH 3305, CH-1015 Lausanne, Switzerland in 2019, Cited 53. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

Amides are ubiquitous molecules in nature and in synthetic chemistry. Here we report a convenient and efficient method to synthesize N-aryl amides via amidation of esters with nitroarenes. In the presence of manganese metal, this amidation proceeded smoothly without the need for additional catalysts or ligands. Various esters and nitroarenes are suitable substrates to afford a wide range of N-aryl amides, including bio-active molecules and intermediates to drug molecules.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Cheung, CW; Shen, N; Wang, SP; Ullah, A; Hu, XL; Ma, JA or concate me.. Application In Synthesis of Methyl 3-phenyl-2-propenoate

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

How did you first get involved in researching Methyl 3-phenyl-2-propenoate

COA of Formula: C10H10O2. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Vucetic, N; Virtanen, P; Nuri, A; Mattsson, I; Aho, A; Mikkola, JP; Salmi, T or concate me.

COA of Formula: C10H10O2. Recently I am researching about COUPLING REACTIONS; EFFICIENT; PHASE; HYDROGENATION; COMPLEXES; MEDIA; SALTS; WATER; BASE; ARYL, Saw an article supported by the Academy of FinlandAcademy of FinlandEuropean Commission [319002, 320115]; Graduate School in Chemical Engineering, Finland. Published in ACADEMIC PRESS INC ELSEVIER SCIENCE in SAN DIEGO ,Authors: Vucetic, N; Virtanen, P; Nuri, A; Mattsson, I; Aho, A; Mikkola, JP; Salmi, T. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

A new bis-layered supported ionic liquid catalyst (SILCA) loaded with palladium was designed and successfully applied for the Heck reaction of iodobenzene and methyl acrylate. The silica modified catalyst consisting of the first ionic liquid layer – covalently anchored imidazolium bromide – on which the second layer, made of pyridine-carboxylic acid balanced with tetramethylguanidinium cation was attached, resulted in a catalyst with high activity. High turnover frequencies of 22,000 h(-1) were achieved in reactions with a low palladium loading as 0.009 mol %. Lower TOFs, indicating on palladium dimerization was detected when higher amounts were used. The TMG cation had a purpose to recapture and stabilize the Pd nanoparticles thus followed a release and catch mechanism. In order to get a full understanding of the catalyst structure and behaviour, the catalyst was characterized by means of nitrogen physisorption, thermal gravimetric analysis, infrared spectroscopy, scanning electron and transmission electron microscopes, solid-state NMR, X-ray photoelectron spectroscopy and inductively coupled plasma spectroscopy. The catalyst preserved good activity in five cycles. (C) 2019 Elsevier Inc. All rights reserved.

COA of Formula: C10H10O2. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Vucetic, N; Virtanen, P; Nuri, A; Mattsson, I; Aho, A; Mikkola, JP; Salmi, T or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Never Underestimate The Influence Of 103-26-4

Product Details of 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Ham, JS; Park, B; Son, M; Roque, JB; Jurczyk, J; Yeung, CS; Baik, MH; Sarpong, R or concate me.

Product Details of 103-26-4. Ham, JS; Park, B; Son, M; Roque, JB; Jurczyk, J; Yeung, CS; Baik, MH; Sarpong, R in [Yeung, Charles S.] Merck & Co Inc, Dept Discovery Chem, Boston, MA 02115 USA; [Park, Bohyun; Son, Mina; Baik, Mu-Hyun] Inst Basic Sci IBS, Ctr Catalyt Hydrocarbon Functionalizat, Daejeon 34141, South Korea; [Park, Bohyun; Son, Mina; Baik, Mu-Hyun] Korea Adv Inst Sci & Technol KAIST, Dept Chem, Daejeon 34141, South Korea; [Ham, Jin Su; Roque, Jose B.; Jurczyk, Justin; Sarpong, Richmond] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA published C-H/C-C Functionalization Approach to N-Fused Heterocycles from Saturated Azacycles in 2020.0, Cited 47.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

Herein we report the synthesis of substituted indolizidines and related N-fused bicycles from simple saturated cyclic amines through sequential C-H and C-C bond functionalizations. Inspired by the Norrish-Yang Type II reaction, C-H functionalization of azacycles is achieved by forming alpha-hydroxy-beta-lactams from precursor alpha-ketoamide derivatives under mild, visible light conditions. Selective cleavage of the distal C(sp(2))-C(sp(3)) bond in alpha-hydroxy-beta-lactams using a Rh-complex leads to alpha-acyl intermediates which undergo sequential Rh-catalyzed decarbonylation, 1,4-addition to an electrophile, and aldol cyclization, to afford N-fused bicycles including indolizidines. Computational studies provide mechanistic insight into the observed positional selectivity of C-C cleavage, which depends strongly on the groups bound to Rh trans to the phosphine ligand.

Product Details of 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Ham, JS; Park, B; Son, M; Roque, JB; Jurczyk, J; Yeung, CS; Baik, MH; Sarpong, R or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Interesting scientific research on Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Haraguchi, R; Yamazaki, T; Torita, K; Ito, T; Fukuzawa, S or concate me.. SDS of cas: 103-26-4

Haraguchi, R; Yamazaki, T; Torita, K; Ito, T; Fukuzawa, S in [Haraguchi, Ryosuke] Chiba Inst Technol, Fac Engn, Dept Appl Chem, 2-17-1 Tsudanuma, Narashino, Chiba 2750016, Japan; [Yamazaki, Tatsuro; Torita, Koki; Ito, Tatsuki; Fukuzawa, Shin-ichi] Chuo Univ, Inst Sci & Engn, Dept Appl Chem, Bunkyo Ku, 1-13-27 Kasuga, Tokyo 1128551, Japan published Planar-chiral ferrocene-based triazolylidene copper complexes: synthesis, characterization, and catalysis in asymmetric borylation of alpha,beta-unsaturated ester in 2020.0, Cited 80.0. SDS of cas: 103-26-4. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

1,2,3-Triazol-5-ylidenes have recently attracted considerable attention as versatile ligands because of their strong electron-donating properties and structural diversities. While some efforts have been devoted to the development of chiral triazolylidene-metal complexes, there is no example achieving asymmetric induction by base-metal complexes with triazolylidene ligands. Herein, we synthesized planar-chiral ferrocene-based triazolylidene copper complexes, which enabled the asymmetric borylation of methyl cinnamate with bis(pinacolato)diboron with good enantioselectivity.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Haraguchi, R; Yamazaki, T; Torita, K; Ito, T; Fukuzawa, S or concate me.. SDS of cas: 103-26-4

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Extended knowledge of C10H10O2

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Qin, M; Wang, QQ; Du, YJ; Shao, LJ; Qi, CZ; Tao, HY or concate me.. Recommanded Product: 103-26-4

An article Encapsulating palladium nanoparticles inside ethylenediamine functionalized and crosslinked chlorinated poly(vinyl chloride) nanofibers as an efficient and stable heterogeneous catalyst for coupling reactions WOS:000567084700018 published article about THERMAL-DECOMPOSITION; RECYCLABLE CATALYST; HECK REACTION; COMPLEX; LIGHT; FIBER in [Qin, Min; Wang, Qingqing; Du, Yijun; Shao, Linjun; Qi, Chenze; Tao, Hongyu] Shaoxing Univ, Zhejiang Key Lab Alternat Technol Fine Chem Proc, Shaoxing 312000, Zhejiang, Peoples R China in 2020.0, Cited 48.0. Recommanded Product: 103-26-4. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Palladium chloride and chlorinated poly (vinyl chloride) (CPVC) mixture were prepared into homogeneous solution, followed by electrospinning to make uniform nanofibers with average diameter of similar to 460 nm. Then, these composite nanofibers were treated in ethylenediamine solution to functionalize and crosslink the CPVC molecules inside the nanofibers to improve their chelating ability and solvent resistance. The functionalization and crosslinking of CPVC molecules inside composite nanofibers were confirmed by SEM, FT-IR, EA and PALS characterizations. The catalytic performance of these palladium encapsulated CPVC nanofibers (Pd@ACPVC) have been evaluated by the Heck and Sonogashira reactions. The catalysis results demonstrate that this Pd@ACPVC catalyst was very effective and stable to catalyze the coupling reaction of aromatic iodides with alkenes (Heck reaction) or phenyl acetylene (Sonogashira reaction) to afford the coupling products in moderate to excellent yields. Due to the regular fibrous structure, the Pd@ACPVC could be readily separated and recovered from reaction mixture. In addition, the Pd@ACPVC could be separately reused for 10 times for Heck reaction and 8 times for Sonogashira reaction without significant decrement of coupling yields. After careful investigation, the palladium leaching from Pd@ACPVC in the reuse procedure could be ascribed to the loss of chelating groups (amino groups) and expansion of free volume holes in the composite nanofibers. The excellent catalytic activity and stability of Pd@ACPVC could be attributed to the strong chelating ability of amino groups, encapsulation of palladium nanoparticles and ultrafine fiber.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Qin, M; Wang, QQ; Du, YJ; Shao, LJ; Qi, CZ; Tao, HY or concate me.. Recommanded Product: 103-26-4

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Now Is The Time For You To Know The Truth About Methyl 3-phenyl-2-propenoate

Formula: C10H10O2. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Huang, Q; Zhang, FY; Liu, S; Jiang, YP; Ouyang, DS or concate me.

An article Systematic investigation of the pharmacological mechanism for renal protection by the leaves of Eucommia ulmoides Oliver using UPLC-Q-TOF/ MS combined with network pharmacology analysis WOS:000670089200002 published article about PERFORMANCE LIQUID-CHROMATOGRAPHY; DIABETIC-NEPHROPATHY; CHEMICAL-CONSTITUENTS; ANTIOXIDANT ACTIVITY; OXIDATIVE STRESS; PATHOGENESIS; PHYTOCHEMISTRY; GLUCOSE; ETHNOPHARMACOLOGY; RESISTANCE in [Huang, Qi; Zhang, Fengyu; Liu, Shao; Jiang, Yueping] Cent South Univ, Xiangya Hosp, Dept Pharm, Changsha 410008, Hunan, Peoples R China; [Huang, Qi; Ouyang, Dongsheng] Cent South Univ, Xiangya Hosp, Dept Clin Pharmacol, Changsha 410008, Hunan, Peoples R China; [Huang, Qi; Ouyang, Dongsheng] Cent South Univ, Inst Clin Pharmacol, Hunan Key Lab Phammcogenet, Changsha 410078, Hunan, Peoples R China; [Huang, Qi; Ouyang, Dongsheng] Changsha Duxact Biotech Co Ltd, Hunan Key Lab Bioanal Complex Matrix Samples, Changsha 411000, Hunan, Peoples R China; [Huang, Qi; Zhang, Fengyu; Liu, Shao; Jiang, Yueping; Ouyang, Dongsheng] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Inst Rat & Safe Medicat Practices, Changsha 410008, Hunan, Peoples R China in 2021.0, Cited 48.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Formula: C10H10O2

Bark is the traditional medicinal component of Eucommia ulmoides Oliver (E. ulmoides). However, the demand for E. ulmoides medicinal materials seriously limits their sustainability. To alleviate resource constraints, the bioactivity of E. ulmoides leaves and its pharmacodynamic basis were investigated. In the present study, extracts of E. ulmoides leaves were found to display potential renal protective properties in rat glomerular mesangial (HBZY-1) cells treated with high levels of glucose, suggesting that they possess potential factors capable of treating diabetic nephropathy. Ultra-performance liquid chromatography tandem quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was used to comprehensively characterize the chemical components of E. ulmoides leaves. A total of 83 possible chemical components, including 12 iridoids, 13 flavonoids, 14 lignans, 20 phenylpropanoids, 14 phenolic acids, and 10 additional components, were identified in E. ulmoides leaves. Network pharmacology was used for a preliminary exploration of the potential mechanism of action of renal protection afforded by E. ulmoides leaves towards diabetic nephropathy. The network pharmacology results were verified using a series of biological experiments. The present study provided the basis for the comprehensive development and utilization of E. ulmoides leaves and the discovery of potential drugs.

Formula: C10H10O2. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Huang, Q; Zhang, FY; Liu, S; Jiang, YP; Ouyang, DS or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

What about chemistry interests you the most Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Ranger, CM; Dzurenko, M; Barnett, J; Geedi, R; Castrillo, L; Ethington, M; Ginzel, M; Addesso, K; Reding, ME or concate me.. Safety of Methyl 3-phenyl-2-propenoate

Safety of Methyl 3-phenyl-2-propenoate. Authors Ranger, CM; Dzurenko, M; Barnett, J; Geedi, R; Castrillo, L; Ethington, M; Ginzel, M; Addesso, K; Reding, ME in SPRINGER published article about in [Ranger, Christopher M.; Barnett, Jenny; Geedi, Ruchika; Reding, Michael E.] ARS, Hort Insects Res Lab, USDA, 1680 Madison Ave, Wooster, OH 44691 USA; [Dzurenko, Marek] Slovak Acad Sci, Inst Forest Ecol, Ludovita Stura 2, Zvolen 96053, Slovakia; [Dzurenko, Marek] Tech Univ Zvolen, Dept Integrated Forest & Landscape Protect, Ul TG Masaryka 24, Zvolen 96001, Slovakia; [Castrillo, Louela] ARS, Emerging Pests & Pathogens Res, USDA, Ithaca, NY 14853 USA; [Ethington, Matthew; Ginzel, Matthew] Purdue Univ, Dept Entomol, 901 W State St, W Lafayette, IN 47907 USA; [Ginzel, Matthew] Purdue Univ, Dept Forestry & Nat Resources, 715 W State St, W Lafayette, IN 47907 USA; [Addesso, Karla] Tennessee State Univ, Coll Agr, Otis L Floyd Nursery Res Ctr, Mcminnville, TN 37110 USA in 2021.0, Cited 54.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Ambrosia beetles (Coleoptera: Scolytinae) cultivate their fungal symbiont within host substrates as the sole source of nutrition on which the larvae and adults must feed. To investigate a possible role for semiochemicals in this interaction, we characterized electrophysiological and behavioral responses of Xylosandrus germanus to volatiles associated with its fungal symbiont Ambrosiella grosmanniae. During still-air walking bioassays, X. germanus exhibited an arrestment response to volatiles of A. grosmanniae, but not antagonistic fungi Beauveria bassiana, Metarhizium brunneum, Trichoderma harzianum, the plant pathogen Fusarium proliferatum, or malt extract agar. Solid phase microextraction-gas chromatography-mass spectrometry identified 2-ethyl-1-hexanol, 2-phenylethanol, methyl benzoate and 3-methyl-1-butanol in emissions from A. grosmanniae; the latter two compounds were also detected in emissions from B. bassiana. Concentration-responses using electroantennography documented weak depolarizations to A. grosmanniae fungal volatiles, unlike the comparatively strong response to ethanol. When tested singly in walking bioassays, volatiles identified from A. grosmanniae elicited relatively weak arrestment responses, unlike the responses to ethanol. Xylosandrus germanus also exhibited weak or no long-range attraction to the fungal volatiles when tested singly during field trials in 2016-2018. None of the fungal volatiles enhanced attraction of X. germanus to ethanol when tested singly; in contrast, 2-phenylethanol and 3-methyl-1-butanol consistently reduced attraction to ethanol. Volatiles emitted by A. grosmanniae may represent short-range olfactory cues that could aid in distinguishing their nutritional fungal symbiont from other fungi, but these compounds are not likely to be useful as long-range attractants for improving detection or mass trapping tactics.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Ranger, CM; Dzurenko, M; Barnett, J; Geedi, R; Castrillo, L; Ethington, M; Ginzel, M; Addesso, K; Reding, ME or concate me.. Safety of Methyl 3-phenyl-2-propenoate

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Interesting scientific research on Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Li, GS; Huang, GW; Sun, RX; Curran, DP; Dai, W or concate me.. Application In Synthesis of Methyl 3-phenyl-2-propenoate

Application In Synthesis of Methyl 3-phenyl-2-propenoate. I found the field of Chemistry very interesting. Saw the article Regioselective Radical Borylation of alpha,beta-Unsaturated Esters and Related Compounds by Visible Light Irradiation with an Organic Photocatalyst published in 2021.0, Reprint Addresses Dai, W (corresponding author), Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China.; Curran, DP (corresponding author), Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15208 USA.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

Radical hydroboration reactions have only recently been reported and are still rare. Here we describe a photoredox radical hydroboration of alpha,beta-unsaturated esters, amides, ketones, and nitriles with NHC-boranes that uses only an organocatalyst and visible light. The conditions are mild, the substrate scope is broad, and the alpha/beta regioselectivity is high. The reaction requires only the organocatalyst; there is no costly metal, and there are no other additives (base, cocatalyst, initiator).

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Li, GS; Huang, GW; Sun, RX; Curran, DP; Dai, W or concate me.. Application In Synthesis of Methyl 3-phenyl-2-propenoate

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics