Category: 103-26-4

Name: Methyl 3-phenyl-2-propenoate. I found the field of Chemistry very interesting. Saw the article Recyclable Copper Nanoparticles-Catalyzed Hydroboration of Alkenes and beta-Borylation of alpha,beta-Unsaturated Carbonyl Compounds with Bis(Pinacolato)Diboron published in 2021.0, Reprint Addresses Bose, SK (corresponding author), JAIN, Ctr Nano & Mat Sci CNMS, Jain Global Campus, Bangalore 562112, Karnataka, India.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

Nano-ferrite-supported Cu nanoparticles (Fe-dopamine-Cu NPs) catalyzed anti-Markovnikov-selective hydroboration of alkenes with B(2)pin(2) is reported under mild reaction conditions. This protocol can be applied to a broad range of substrates with high functional group compatibility. In addition, we demonstrated the use of Fe-dopamine-Cu NPs as a catalyst for the beta-borylation of alpha,beta-unsaturated ketones and ester, providing alkylboronate esters in up to 98% yield. Reuse of the magnetically recyclable catalyst resulted in no significant loss of activity in up to five reaction runs for both systems.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Shegavi, ML; Saini, S; Bhawar, R; Vishwantha, MD; Bose, SK or concate me.. Name: 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

Recommanded Product: 103-26-4. Authors Shibutani, S; Nagao, K; Ohmiya, H in AMER CHEMICAL SOC published article about in [Shibutani, Shotaro; Nagao, Kazunori; Ohmiya, Hirohisa] Kanazawa Univ, Grad Sch Med Sci, Div Pharmaceut Sci, Kanazawa, Ishikawa 9201192, Japan; [Ohmiya, Hirohisa] PRESTO, JST, Kawaguchi, Saitama 3320012, Japan in 2021.0, Cited 62.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

This manuscript describes a visible-light-mediated organo-photoredox catalytic process for vicinal difunctionalization of alkenes using heteroatom nucleophiles and aliphatic redox active esters. A wide range of heteroatom nucleophiles including alcohols, water, carboxylic acids, amides, and halogens can be used for this reaction. This radical relay type reaction allows forging of C(sp(3))-C(sp(3)) with a carbon centered radical and C(sp(3))-heteroatom bonds with a benzyl cation on the vinylarenes with complete regioselectivity in a single step.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Shibutani, S; Nagao, K; Ohmiya, H 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

Application In Synthesis of Methyl 3-phenyl-2-propenoate. Authors Steele, JH; Bozor, MX; Boyce, GR in AMER CHEMICAL SOC published article about in [Steele, Jacob H.; Bozor, Marie X.; Boyce, Gregory R.] Florida Gulf Coast Univ, Dept Chem & Phys, Ft Myers, FL 33965 USA in 2020.0, Cited 23.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

The synthesis of a commercial fragrance, methyl cinnamate, via Fischer esterification was evaluated for use as a second-year organic chemistry course. The experiment utilizes trans-cinnamic acid, a commercial flavoring that possesses a mild honey floral odor, as an inexpensive starting material. Both the starting material and the product are listed as GRAS (Generally Recognized as Safe) for use in foods and fragrances. The high-yielding experiment enables students to explore concepts of flavor and fragrances, transmutation of scent, catalysis, green chemistry, NMR spectroscopy, thin layer chromatography (TLC), and acid-base extractions. In addition to the commonly employed sulfuric acid catalyst, alternative conditions were developed using p-toluenesulfonic acid monohydrate as an easier to handle catalyst, and conditions for performing both reactions under microwave irradiation are also reported. The experiment was analyzed in a second-year organic chemistry laboratory over six semesters.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Steele, JH; Bozor, MX; Boyce, GR 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

An article Variation of floral volatiles and fragrance reveals the phylogenetic relationship among nine wild tree peony species WOS:000504299200001 published article about DIFFERENT CULTIVATION REGIONS; GRANDIS L. OSBECK; ESSENTIAL OIL; PHENOTYPIC SELECTION; GAS-CHROMATOGRAPHY; BIOSYNTHESIS; SCENT; POLLINATION; FRUIT in [Luo, Xiaoning; Yuan, Meng; Li, Bingjie; Li, Chenyao; Zhang, Yanlong; Shi, Qianqian] Northwest A&F Univ, Coll Landscape Architecture & Art, Yangling, Shaanxi, Peoples R China in 2020.0, Cited 64.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Quality Control of Methyl 3-phenyl-2-propenoate

In recent years, more and more attention has been paid to the natural floral volatiles in tree peony and the fragrance components have been widely used in the fields of health care, perfumes, and cosmetics. However, there is little research on the identification of fragrance components of wild tree peony species. In present study, volatile components in petals of nine wild tree peony species were analyzed using a headspace solid-phase microextraction (SPME) technique coupled with gas chromatography-mass spectrometry (GC-MS). A total of 124 volatile components were identified and clustered into five major chemical classes: terpenoids, alkanes, alcohols, aldehydes, and ketones. Overall, combined with the sensory evaluation of nine wild tree peony species, Paeonia. ostii (P2) performed herbal and waxy attributes, mainly dominated by hexanal and pentadecane, respectively. P rockii (P1), P qiui (P3), P jishanensis (P4), and P decomposita (P5) all possessed sweet attribute, which was positively correlated with geraniol and citronellol. P delavayi (P9), P lutea (P7), P ludlowii (P8), and P potanini (P6) performed intense floral attribute dominated by linalool and trans-linalool oxide. Moreover, the results of principal component analysis (PCA) and hierarchical clustering analysis (HCA) showed P decomposita (P5), P qiui (P3), P rockii (P1), P jishanensis (P4), and P ostii (P2) in the Subsect. Vagiatae were mixed to form one cluster while P lutea (P7), P delavayi (P9), P ludlowii (P8), and P potanini (P6) in the Subsect. Delavayanae formed the other cluster. In terms of geographical distribution, the two clusters are consistent with the distribution of wild tree peony species. The present study clarified the relationship between fragrance and components and further revealed the phylogenetic relationship of nine wild tree peony species, thus providing a theoretical basis for their development and utilization.

Quality Control of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Luo, XN; Yuan, M; Li, BJ; Li, CY; Zhang, YL; Shi, QQ 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

I found the field of Science & Technology – Other Topics very interesting. Saw the article Merging shuttle reactions and paired electrolysis for reversible vicinal dihalogenations published in 2021.0. Computed Properties of C10H10O2, Reprint Addresses Morandi, B (corresponding author), Swiss Fed Inst Technol, Lab Organ Chem, Dept Chem & Appl Biosci, Zurich, Switzerland.; Waldvogel, SR (corresponding author), Johannes Gutenberg Univ Mainz, Dept Chem, Mainz, Germany.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

Vicinal dibromides and dichlorides are important commodity chemicals and indispensable synthetic intermediates in modern chemistry that are traditionally synthesized using hazardous elemental chlorine and bromine. Meanwhile, the environmental persistence of halogenated pollutants necessitates improved approaches to accelerate their remediation. Here, we introduce an electrochemically assisted shuttle (e-shuttle) paradigm for the facile and scalable interconversion of alkenes and vicinal dihalides, a class of reactions that can be used both to synthesize useful dihalogenated molecules from simple alkenes and to recycle waste material through retro-dihalogenation. The reaction is demonstrated using 1,2-dibromoethane, as well as 1,1,1,2-tetrachloroethane or 1,2-dichloroethane, to dibrominate or dichlorinate, respectively, a wide range of alkenes in a simple setup with inexpensive graphite electrodes. Conversely, the hexachlorinated persistent pollutant lindane could be fully dechlorinated to benzene in soil samples using simple alkene acceptors.

Computed Properties of C10H10O2. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Dong, XC; Roeckl, JL; Waldvogel, SR; Morandi, B 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

I found the field of Agriculture very interesting. Saw the article Impact evaluation of growth stage and species on morpho-physiological traits and bioactive constituent of essential oil in Ocimum through multi-year experiment published in 2020.0. Recommanded Product: Methyl 3-phenyl-2-propenoate, Reprint Addresses Sakure, AA (corresponding author), Anand Agr Univ, Dept Agr Biotechnol, Anand, Gujarat, India.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

The genus Ocimum displays excellent variability among the species and sub-species due to the highly crosspollinated nature and interspecific hybridization. The present investigation was carried out to identify the commercially promising growth stage(s) in different Ocimum for exatraction of oil and bioactive compounds at heighest. A set of three cultivated species were evaluated to study the variation in morpho-physiological traits and essential oil composition harvested at three stages namely vegetative, flowering and seed setting stage. The experiment was conducted for three consecutive years in factorial randomized complete block design with three replicates. The analysis of variance exhibited that the individual effect of Ocimum species and growth stage along with their interaction effect was significant in all the morpho-physiological parameters and bioactive constituent of oil in a pooled analysis. Highest plant height (103.95 cm) was observed in O. gratissimum L. harvested at seed setting stage while harvesting at flowering stage exhibited maximum leaf area (26.80 cm(2)), oil (0.52 %) and eugenol content (85.82 %). Sweet basil harvested at seed setting stage disclosed maximum branches per plant (21.53) and leaves per plant (4949) although linalool content (47.99 %) was found highest in harvested at flowering stage. O. basilicum L. was detected a great source of methyl chavicol (7.48 %) though this species was weaker source for methyl cinnamate. Among the studied species, O. gratissimum showed a negligible amount of methyl eugenol content in oil. A positive correlation between the morpho-physiological traits, oil content and its constituents with the various growth stages were recorded. None of bioactive compounds exhibited any correlation with oil content. Principle component analysis revealed that of the total variation, O. gratissimum contributed maximum (61.58 %) variation followed by O. basilicum (35.36 %). The results of current study suggested that the different Ocimum species can be harvest at various growth stages to get the maximum yield and target chemical compounds based on the needy industrial value.

Recommanded Product: Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Thounaojam, AS; Sakure, AA; Dhaduk, HL; Kumar, S; Mistry, JG 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

COA of Formula: C10H10O2. Authors Ishida, N; Kamae, Y; Ishizu, K; Kamino, Y; Naruse, H; Murakami, M in AMER CHEMICAL SOC published article about in [Ishida, Naoki; Kamae, Yoshiki; Ishizu, Keigo; Kamino, Yuka; Naruse, Hiroshi; Murakami, Masahiro] Kyoto Univ, Dept Synthet Chem & Biol Chem, Kyoto 6158510, Japan in 2021.0, Cited 35.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Herein described is a sustainable system for hydrogenation that uses solar light as the ultimate source of energy. The system consists of two steps. Solar energy is captured and chemically stored in the first step; exposure of a solution of azaxanthone in ethanol to solar light causes an energy storing dimerization of the ketone to produce a sterically strained 1,2-diol. In the second step, the chemical energy stored in the vicinal diol is released and used for hydrogenation; the diol offers hydrogen onto alkenes and splits back to azaxanthone, which is easily recovered and reused repeatedly for capturing solar energy.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Ishida, N; Kamae, Y; Ishizu, K; Kamino, Y; Naruse, H; Murakami, M or concate me.. COA of Formula: C10H10O2

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

Authors Von Tokarski, F; Lemaignen, A; Portais, A; Fauchier, L; Hennekinne, F; Sautenet, B; Halimi, JM; Legras, A; Patat, F; Bourguignon, T; Mirguet, C; Bernard, A; Bernard, L in ELSEVIER SCI LTD published article about STAPHYLOCOCCUS-AUREUS; BACTERIAL-ENDOCARDITIS; MANAGEMENT; IMPACT in [Von Tokarski, Florent; Lemaignen, Adrien; Portais, Antoine; Bernard, Louis] Serv Med Interne & Malad Infect, Tours, France; [Von Tokarski, Florent; Sautenet, Benedicte; Halimi, Jean-Michel] Serv Nephrol HTA Dialyses Transplantat Renale, Tours, France; [Fauchier, Laurent; Bernard, Anne] Serv Cardiol, Tours, France; [Hennekinne, Fanny] Serv Geriatrie, Tours, France; [Legras, Annick] Serv Med Intens, Tours, France; [Patat, Frederic] Serv Echog, Tours, France; [Bourguignon, Thierry] Serv Chirurg Cardiovasc, Tours, France; [Mirguet, Christian] CHRU Tours, Serv Reanimat Cardiovasc, Tours, France in 2020.0, Cited 27.0. Quality Control of Methyl 3-phenyl-2-propenoate. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Objectives: The incidence of acute kidney injury (AKI) in infective endocarditis (IE), its risk factors and consequences on patient and renal survival remain debated. Methods: Patients hospitalized for a first episode of IE (possible or definite according to modified Duke criteria) between 2013 and 2016 were included. The primary endpoint was to determine risk factors for early AKI (E-AKI) during the first week of management of IE. Results: A total of 276 patients were included: 220 (79.7%) had definite IE and 56 (20.3%) had possible IE. E-AKI occurred in 150 patients (53%). IE due to Staphylococcus aureus (OR 3.41; 95% CI 1.83-6.39; p < 0.01), history of diabetes (OR 2.34; 95% CI 1.25-4.37; p < 0.01), peripheral arterial disease (OR 2.59; 95% CI 1.07-6.23; p < 0.05), immunological manifestations (OR 3.11; 95% CI 1.31-7.39; p = 0.01), and use of norepinephrine (OR 3.44; 95% CI 1.72-7.02; p < 0.01) were associated with E-AKI. In subgroup analysis, infectious disease consultation was associated with a lower risk of AKI at day 7 (OR 0.41; 95% CI 0.16-0.88; p = 0.04). E-AKI was associated with 1-year mortality (OR 1.65; 95% CI 1.03-2.64; p = 0.04) and chronic kidney disease progression (OR 2.23; 95% CI 1.30-3.82; p < 0.01). Conclusions: E-AKI is common in IE and often associated with non-modifiable variables. Multidisciplinary management should be mandatory, and awareness of AKI diagnosis and etiological explorations should be raised. (C) 2020 The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. Quality Control of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Von Tokarski, F; Lemaignen, A; Portais, A; Fauchier, L; Hennekinne, F; Sautenet, B; Halimi, JM; Legras, A; Patat, F; Bourguignon, T; Mirguet, C; Bernard, A; Bernard, 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,
Ester – an overview | ScienceDirect Topics

Application In Synthesis of Methyl 3-phenyl-2-propenoate. In 2019.0 CHEM SCI published article about HETEROCYCLIC CARBENE BORANES; NMR COUPLING-CONSTANTS; CATALYZED HYDROBORATION; CARBONYL-COMPOUNDS; EFFICIENT; INSERTION; ALKENES; ADDITIONS; ALDEHYDES; ADDUCTS in [Radcliffe, James E.; Fasano, Valerio; Adams, Ralph W.; You, Peiran; Ingleson, Michael J.] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England in 2019.0, Cited 44.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

Useful alpha-boryl esters can be synthesized in one step from alpha,beta-unsaturated esters using just a simple to access NHC-BH3 (NHC = N-heterocyclic carbene) and catalytic I-2. The scope of this reductive alpha-borylation methodology is excellent and includes a range of alkyl, aryl substituted and cyclic and acyclic alpha,beta-unsaturated esters. Mechanistic studies involving reductive borylation of a cyclic alpha,beta-unsaturated ester with NHC-BD3/I-2 indicated that concerted hydroboration of the alkene moiety in the alpha,beta-unsaturated ester proceeds instead of a stepwise process involving initial 1,4-hydroboration; this is in contrast to the recently reported reductive alpha-silylation. The BH2(NHC) unit can be transformed into electrophilic BX2(NHC) moieties (X = halide) and the ester moiety can be reduced to the alcohol with the borane unit remaining intact to form b-boryl alcohols. The use of a chiral auxiliary, 8-phenylmenthyl ester, also enables effective stereo-control of the newly formed C-B bond. Combined two step ester reduction/borane oxidation forms diols, including excellent e. e. (97%) for the formation of S-3-phenylpropane-1,2-diol. This work represents a simple transition metal free route to form bench stable alpha-boryl esters from inexpensive starting materials.

Application In Synthesis of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Radcliffe, JE; Fasano, V; Adams, RW; You, PR; Ingleson, MJ 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

Safety of Methyl 3-phenyl-2-propenoate. Recently I am researching about MIZOROKI-HECK; CO; NANOPARTICLES; CHEMISTRY; LIGANDS; HALIDES; OXIDE, Saw an article supported by the . Published in ELSEVIER in AMSTERDAM ,Authors: Hajipour, AR; Khorsandi, Z; Abeshtian, Z. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

A novel, biodegradable and environmental friendly magnetic cross-linked chitosan fibers and its cobalt complex was prepared and characterized by various techniques such as FT-IR, SEM, EDX, Elemental mapping, TEM, TGA, XRD and VSM analysis. This palladium and phosphine-free catalyst was found as a highly active heterogeneous catalyst for Heck and Sonogashira reactions in green media. The catalyst was easily separated using an external magnet and the recovered catalyst was reused for six cycles without significant loss of catalytic activity.

Safety of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Hajipour, AR; Khorsandi, Z; Abeshtian, Z 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