Category: 103-26-4

COA of Formula: C10H10O2. I found the field of Biochemistry & Molecular Biology; Plant Sciences very interesting. Saw the article Biosynthesis of methyl (E)-cinnamate in the liverwort Conocephalum salebrosum and evolution of cinnamic acid methyltransferase published in 2019, Reprint Addresses Chen, F (corresponding author), Univ Tennessee, Dept Plant Sci, Knoxville, TN 37996 USA.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

Methyl (E)-cinnamate is a specialized metabolite that occurs in a variety of land plants. In flowering plants, it is synthesized by cinnamic acid methyltransferase (CAMT) that belongs to the SABATH family. While rarely reported in bryophytes, methyl (E)-cinnamate is produced by some liverworts of the Conocephalum conicum complex, including C. salebrosum. In axenically grown thalli of C. salebrosum, methyl (E)-cinnamate was detected as the dominant compound. To characterize its biosynthesis, six full-length SABATH genes, which were designated CsSABATH1-6, were cloned from C. salebrosum. These six genes showed different levels of expression in the thalli of C. salebrosum. Next, CsSABATH1-6 were expressed in Escherichia coli to produce recombinant proteins, which were tested for methyltransferase activity with cinnamic acid and a few related compounds as substrates. Among the six SABATH proteins, CsSABATH6 exhibited the highest level of activity with cinnamic acid. It was renamed CsCAMT. The apparent Km value of CsCAMT using (E)-cinnamic acid as substrate was determined to be 50.5 mu M. In contrast, CsSABATH4 was demonstrated to function as salicylic acid methyltransferase and was renamed CsSAMT. Interestingly, the CsCAMT gene from a sabinene-dominant chemotype of C. salebrosum is identical to that of the methyl (E)-cinnamate-dominant chemotype. Structure models for CsCAMT, CsSAMT and one flowering plant CAMT (ObCCMT1) in complex with (E)-cinnamic acid and salicylic acid were built, which provided structural explanations to substrate specificity of these three enzymes. In phylogenetic analysis, CsCAMT and ObCCMT1 were in different clades, implying that methyl (E)-cinnamate biosynthesis in bryophytes and flowering plants originated through convergent evolution.

Welcome to talk about 103-26-4, If you have any questions, you can contact Zhang, C; Chen, XL; Crandall-Stoder, B; Qian, P; Kollner, TG; Guo, H; Chen, F or send Email.. 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

Name: Methyl 3-phenyl-2-propenoate. In 2021.0 ORG LETT published article about INSERTION in [Li, Guosong; Huang, Guanwang; Sun, Ruixia; Dai, Wen] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China; [Curran, Dennis P.] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15208 USA in 2021.0, Cited 28.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

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).

Welcome to talk about 103-26-4, If you have any questions, you can contact Li, GS; Huang, GW; Sun, RX; Curran, DP; Dai, W or send Email.. 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

Authors Tamang, SR; Singh, A; Bedi, D; Bazkiaei, AR; Warner, AA; Glogau, K; McDonald, C; Unruh, DK; Findlater, M in NATURE RESEARCH published article about CHEMOSELECTIVE REDUCTION; SECONDARY AMIDES; TERTIARY AMIDES; MILD; ALDEHYDES; ALCOHOLS; COMPLEX; AMINES; HYDROGENATION; HYDROSILANES in [Tamang, Sem Raj; Singh, Arpita; Bedi, Deepika; Bazkiaei, Adineh Rezaei; Warner, Audrey A.; Glogau, Keeley; McDonald, Corey; Unruh, Daniel K.; Findlater, Michael] Texas Tech Univ, Dept Chem & Biochem, Lubbock, TX 79409 USA in 2020, Cited 69. Product Details of 103-26-4. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Catalytic reduction of carboxamides into their corresponding amines is an attractive but extremely challenging transformation, which often meets with limited success; the valuable amine products drive ongoing research in this area. Here we show the direct deoxygenation of carboxamides using earth-abundant lanthanum catalysts in the presence of HBpin, presenting good to excellent yields with broad substrate scope and functional group/heteroatom tolerance. Moreover, this method is also effective in catalysing the hydroboration of esters. Finally, selective cleavage of the amide group bonds (C-N versus C-O) could be achieved based on the nature of the nitrogen substituents. Amide reduction via hydroboration is challenging, and catalysts often exhibit limited substrate scope. Here the authors report synthesis of a lanthanum cluster as a catalyst for the hydroboration of esters and amides, capable of reducing a wide range of primary, secondary and tertiary amides to amines.

Bye, fridends, I hope you can learn more about C10H10O2, If you have any questions, you can browse other blog as well. See you lster.. Product Details of 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

An article Controlled Radical Copolymerization of Cinnamic Derivatives as Renewable Vinyl Monomers with Both Acrylic and Styrenic Substituents: Reactivity, Regioselectivity, Properties, and Functions WOS:000456349600016 published article about SINGLE-ELECTRON TRANSFER; NATURALLY-OCCURRING TERPENES; RAFT POLYMERIZATION; TEMPERATURE-DEPENDENCE; METHYL-METHACRYLATE; RUTHENIUM COMPLEXES; ESSENTIAL OILS; SET-LRP; POLYMERS; FUTURE in [Terao, Yuya; Satoh, Kotaro; Kamigaito, Masami] Nagoya Univ, Grad Sch Engn, Dept Mol & Macromol Chem, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan in 2019.0, Cited 105.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Application In Synthesis of Methyl 3-phenyl-2-propenoate

A series of cinnamic monomers, which can be derived from naturally occurring phenylpropanoids, were radically copolymerized with vinyl monomers such as methyl acrylate (MA) and styrene (St). Although the monomer reactivity ratios were close to zero for all the cinnamic monomers, such as methyl cinnamate (CAMe), cinnamic acid (CA), N-isopropyl cinnamide (CNIPAm), cinnamaldehyde (CAld), and cinnamonitrile (CN), they were incorporated into the copolymers and significantly increased the glass transition temperatures despite the relatively low incorporation rates of up to 40 mol % due to their rigid 1,2-disubstituted structures. The regioselectivity of the radical copolymerization of CAMe was evaluated on the basis of the results of ruthenium-catalyzed atom transfer radical additions as model reactions. The obtained products suggest that the radicals of MA and St predominantly attack the vinyl carbon of the carbonyl side of CAMe and that the propagation of CAMe mainly occurs via the styrenic radical. The ruthenium-catalyzed living radical polymerization, nitroxide-mediated polymerization (NMP), and reversible addition-fragmentation chain transfer (RAFT) polymerization provided the copolymers with controlled molecular weights, narrow molecular weight distributions, and controlled comonomer compositions. The copolymers of N-isopropylacrylamide (NIPAM) and CNIPAm prepared via RAFT copolymerization showed thermoresponsivity with a lower critical solution temperature (LCST) that could be tuned by altering the comonomer incorporation and a higher LCST than the copolymers of NIPAM and St, which possessed similar molecular weights and similar NIPAM contents, due to the additional N-isopropylamide groups in the CNIPAm units compared to the St units.

Application In Synthesis of Methyl 3-phenyl-2-propenoate. Welcome to talk about 103-26-4, If you have any questions, you can contact Terao, Y; Satoh, K; Kamigaito, M or send Email.

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 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. 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

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.

Quality Control of Methyl 3-phenyl-2-propenoate. Welcome to talk about 103-26-4, If you have any questions, you can contact Steele, JH; Bozor, MX; Boyce, GR or send Email.

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. I found the field of Chemistry; Engineering very interesting. Saw the article Supercritical CO2 extraction and selective adsorption of aroma materials of selected spice plants in functionalized silica aerogels published in 2019.0, Reprint Addresses Lazar, I (corresponding author), Univ Debrecen, Dept Inorgan & Analyt Chem, Egyet Ter 1, H-4032 Debrecen, Hungary.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

Static supercritical fluid extraction has been used to concentrate the aroma materials of common herbs and spices. The technique has provided a higher number of components and cleaner extract than the one-step ethanol maceration. The one-step supercritical fluid extraction of the aroma compounds has been combined with their in situ adsorption in hydrophilic and hydrophobic silica aerogels. The extracts have been analyzed by a GC-MS technique and 55 aroma compounds have been identified. Most of the compounds have been adsorbed in both polar and apolar silica aerogels with no direct connection with the surface polarity. However, previously undetected compounds enriched to an analytically significant level, while others competed with each other for the active sites on the surface. Functionalized silica aerogels can be used as a new type of aroma storage materials and as selective and tuneable adsorbents for the extraction and enrichment of potentially active components from a complex matrix.

Application In Synthesis of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Gyori, E; Varga, A; Fabian, I; Lazar, I 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

In 2019.0 ORGANOMETALLICS published article about ENANTIOSELECTIVE SYNTHESIS; BOND ACTIVATION; ARYL ETHERS; ALKYLATION; CYCLOADDITION; FLAVONOIDS; ALKYNES; ALKENYLATION; CYCLIZATION; ALCOHOLS in [Mokar, Bhanudas Dattatray; Yi, Chae S.] Marquette Univ, Dept Chem, Milwaukee, WI 53233 USA in 2019.0, Cited 62.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Recommanded Product: 103-26-4

Chromene and benzoxacyclic derivatives were efficiently synthesized from the ruthenium-catalyzed dehydrative C-H coupling reaction of phenols with alpha,beta-unsaturated carbonyl compounds. The cationic ruthenium-hydride complex was found to be an effective catalyst for the coupling and annulation of phenols with enals to form chromene products. The coupling of phenols with linear enones afforded 2,4-disubstituted chromene derivatives, whereas the analogous coupling with cyclic enones yielded 9-hydroxybenzoxazole products. The reaction of 3,5-dimethoxyphenol with PhCH=CHCDO resulted in the chromene product with a significant H/D exchange to both benzylic and vinyl positions. The most significant carbon isotope effect from the coupling of 3,5-dimethoxyphenol with 4-methoxycinnamaldehyde was observed on the a-olefinic carbon of the chromene product (C(2) = 1.067). A Hammett plot from the coupling of 3,5-dimethoxyphenol with para-substituted p-X-C6H4CH=CHCHO displayed a linear correlation, with a strong promotional effect by an electron -withdrawing group (rho = +1.5; X = OCH3, CH3, H, F, Cl). Several biologically active chromenone derivatives were synthesized by using the catalytic coupling method. The catalytic method provides an expedient synthetic protocol for the coupling of phenols with alpha,beta-unsaturated carbonyl compounds without employing reactive reagents or forming any wasteful byproducts.

Recommanded Product: 103-26-4. Welcome to talk about 103-26-4, If you have any questions, you can contact Mokar, BD; Yi, CS or send Email.

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 Palladium (II) anchored on a magnetic mesoporous polymelamine-formaldehyde as new catalyst for Heck coupling reaction: optimization of reaction using response surface methodology WOS:000512810900011 published article about CONJUGATED MICROPOROUS POLYMER; HETEROGENEOUS CATALYST; EFFICIENT CATALYST; ORGANIC POLYMERS; NANOPARTICLES; COMPLEX; HYDROGENATION; NANOCATALYST; SILICA; PD in [Shahamat, Zahra; Nemati, Firouzeh; Elhampour, Ali] Semnan Univ, Dept Chem, Semnan, Iran in 2020.0, Cited 59.0. COA of Formula: C10H10O2. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

The paper describes synthesis of a novel mesoporous and magnetically regenerated heterogeneous nanocatalyst with high catalytic activity. The synthesis strategy includes a one-step polycondensation reaction of melamine, formaldehyde and FeCl3 center dot 6H(2)O in a simple and sustainable manner and followed by immobilization of Pd(II) on it. Formation and properties of nanocomposite were characterized by different techniques; the results were illustrated good surface area and a well-defined mesopore structure. Also the palladium-catalyzed C-C bond formation between aryl halides and olefins was selected to survey the activity of the synthesized nanocatalyst. Central Composite Design (CCD) strategy was used to predict the optimum synthesis conditions and identify the remarkable and effective factors including temperature, period of the reaction and amount of catalyst. These results were also verified experimentally. In order to minimize systematic error, the experimental runs as a randomized fashion were accomplished.

COA of Formula: C10H10O2. Bye, fridends, I hope you can learn more about C10H10O2, If you have any questions, you can browse other blog as well. See you lster.

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

Formula: C10H10O2. Authors Steingass, CB; Dickreuter, J; Kuebler, S; Schweiggert, RM; Carle, R in SPRINGER published article about in [Steingass, Christof B.; Schweiggert, Ralf M.] Geisenheim Univ, Dept Beverage Res, Chair Anal & Technol Plant Based Foods, Von Lade Str 1, D-65366 Geisenheim, Germany; [Steingass, Christof B.; Dickreuter, Jennifer; Kuebler, Sabine; Carle, Reinhold] Univ Hohenheim, Inst Food Sci & Biotechnol, Chair Plant Foodstuff Technol & Anal, Garbenstr 25, D-70599 Stuttgart, Germany; [Kuebler, Sabine] Wala Heilmittel GmbH, Dorfstr 1, D-73087 Bad Boll Eckwalden, Germany; [Carle, Reinhold] King Abdulaziz Univ, Dept Biol Sci, Fac Sci, POB 80257, Jeddah 21589, Saudi Arabia in 2021.0, Cited 24.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Green-ripe pineapples are shipped overseas by sea freight, while those picked at full maturity need to be transported by airfreight over the same large distance. In this study, fresh-cut pineapple cubes were assessed two, five, and eight days after processing from green-ripe pineapples after mimicked sea freigh (SF) and fully ripe air-freighted (AF) pineapples. The sea-freighted samples displayed elevated titratable acidity (TA), thus resulting in smaller ratios of total soluble solids and TA compared to the AF pineapples. Differences in the carotenoid levels of the two fresh-cut categories were found to be insignificant. By contrast, hierarchical cluster analysis (HCA) and principal component analysis (PCA) calculated on the basis of the volatiles analysed by headspace solid-phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) permitted to distinguish all six individual sample types and to segregate them into two major clusters (SF and AF). The effect of storage on the volatiles was further evaluated by partial least squares (PLS) regression. Substantial chemical markers to differentiate the individual samples and to describe the effect of storage were deduced from the PCA and PLS regression, respectively. In general, fresh-cut products obtained from fully ripe AF fruit displayed higher concentrations of volatiles, in particular, increased concentrations of diverse methyl esters. With progressing storage duration, the concentrations of ethanol and diverse ethyl esters increased. Moreover, products from AF pineapples displayed lower microbial counts compared to those from SF fruit.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Steingass, CB; Dickreuter, J; Kuebler, S; Schweiggert, RM; Carle, R or concate me.. 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

Recommanded Product: 103-26-4. Lyczko, J; Masztalerz, K; Lipan, L; Lech, K; Carbonell-Barrachina, AA; Szumny, A in [Lyczko, Jacek; Szumny, Antoni] Wroclaw Univ Environm & Life Sci, Fac Biotechnol & Food Sci, PL-50375 Wroclaw, Poland; [Masztalerz, Klaudia; Lech, Krzysztof] Wroclaw Univ Environm & Life Sci, Inst Agr Engn, PL-51630 Wroclaw, Poland; [Lipan, Leontina; Carbonell-Barrachina, Angel A.] Univ Miguel Hernandez Elche, Dept Agrofood Technol, Escuela Politecn Super Orihuela, Alicante 03312, Spain published Chemical determinants of dried Thai basil (O. basilicum var. thyrsiflora) aroma quality in 2020.0, Cited 34.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

Herbs market is constantly growing worldwide, and is trying to find new species and varieties coming from specific geographical regions. While the increasing production demands novel solutions for product preservation, consumers demand guaranteed quality for these products. In case of herbs, the most common preservation method is thermo-based process – drying, which strongly affects products quality. Regarding the technological possibilities and efficiency, convective drying (CD), microwave drying, vacuum-microwave drying (VMD) and combined convective pre-drying followed by vacuum-microwave finish-drying (CPD-VMFD) methods are the most popular ones. In this study, the influence of the drying methods (CD, VMD and CPD-VMD) on Thai basil (O. basilicum var. thyrsiflora) quality was evaluated for the very first time. The chemical composition of their essential oils (EOs), dried samples (aroma profiles, APs) and sensory quality of the dried products were also studied. As a result of multiple chemical and sensory analyses and after cross-checking all these results, guidelines for chemical markers of Thai basil aroma quality were established. Odour-active compounds (OACs) contribution in Thai basil EOs did not show a clear pattern to link it with quality assessments; however, OACs contribution in APs did. The drying treatments leading to the dried products with the highest quality were: (i) 2 h CPD at 50 degrees C followed by VMFD with 360 W (2 h CPD50) and (ii) 1 h CPD at 70 degrees C followed by VMFD with 360 W (1 h CPD70).

Recommanded Product: 103-26-4. Bye, fridends, I hope you can learn more about C10H10O2, If you have any questions, you can browse other blog as well. See you lster.

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