Our Top Choice Compound:C10H10O2

Computed Properties of C10H10O2. 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.

An article Biosynthesis of methyl (E)-cinnamate in the liverwort Conocephalum salebrosum and evolution of cinnamic acid methyltransferase WOS:000475996800006 published article about ESSENTIAL OIL COMPOSITION; BIOCHEMICAL-CHARACTERIZATION; CARBOXYL METHYLTRANSFERASE; ARABIDOPSIS-THALIANA; TERPENE SYNTHASES; INDOLE-3-ACETIC-ACID METHYLTRANSFERASE; SABATH METHYLTRANSFERASES; MOLECULAR-CLONING; VOLATILE; SALICYLATE in [Zhang, Chi; Chen, Xinlu; Chen, Feng] Univ Tennessee, Dept Plant Sci, Knoxville, TN 37996 USA; [Crandall-Stoder, Barbara] Southern Illinois Univ, Dept Plant Biol, Carbondale, IL 62901 USA; [Qian, Ping] Shandong Agr Univ, Chem & Mat Sci Fac, Tai An 271018, Shandong, Peoples R China; [Koellner, Tobias G.] Max Planck Inst Chem Ecol, Dept Biochem, Hans Knoll Str 8, D-07745 Jena, Germany; [Guo, Hong] Univ Tennessee, Dept Biochem Cellular & Mol Biol, Knoxville, TN 37996 USA; [Guo, Hong] Oak Ridge Natl Lab, UT ORNL Ctr Mol Biophys, Oak Ridge, TN 37830 USA in 2019, Cited 63. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Computed Properties of C10H10O2

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.

Computed Properties of C10H10O2. 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.

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

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Product Details of 103-26-4. Welcome to talk about 103-26-4, If you have any questions, you can contact Saavedra, B; Gonzlez-Gallardo, N; Meli, A; Ramn, DJ or send Email.

An article A Bipyridine-Palladium Derivative as General Pre-Catalyst for Cross-Coupling Reactions in Deep Eutectic Solvents WOS:000476320300001 published article about SONOGASHIRA COUPLINGS; PD; EFFICIENT; SYSTEM in [Saavedra, Beatriz; Gonzalez-Gallardo, Nerea; Meli, Alessandro; Ramon, Diego J.] Univ Alicante, Fac Ciencias, Dept Quim Organ, Apdo 99, Alicante 03080, Spain; [Saavedra, Beatriz; Gonzalez-Gallardo, Nerea; Meli, Alessandro; Ramon, Diego J.] Univ Alicante, Fac Ciencias, ISO, Apdo 99, E-03080 Alicante, Spain; [Meli, Alessandro] Univ Palermo, Dipartimento Sci Biol Chim & Farmaceut, Viale Sci,Ed 17, I-90128 Palermo, Italy in 2019.0, Cited 34.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Product Details of 103-26-4

A versatile and DES-compatible bipyridine palladium complex has been developed as a general pre-catalyst for different cross-coupling reactions (Hiyama, Suzuki-Miyaura, Heck-Mizoroki and Sonogashira) in deep eutectic solvents. Hydrogen bond capacity of the ligand allows to keep the excellent level of results previously obtained in classical organic solvents. Palladium pre-catalyst showed a high catalytic activity for many cross-coupling reactions, demonstrating a great versatility and applicability. Also, this methodology employs sustainable solvents as a reaction medium and highlights the potential of DES as alternative solvents in organometallic catalysis. The catalyst and DES were easily and successfully recycled. The formation of PdNPs in DES has been confirmed by TEM and XPS analysis and their role as catalyst by mercury test. The dynamic coordination of bipyridine-type ligand in the palladium complex formation has been studied via UV/Vis.

Product Details of 103-26-4. Welcome to talk about 103-26-4, If you have any questions, you can contact Saavedra, B; Gonzlez-Gallardo, N; Meli, A; Ramn, DJ 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

What advice would you give a new faculty member or graduate student interested in a career 103-26-4

Welcome to talk about 103-26-4, If you have any questions, you can contact Komarova, AO; Dick, GR; Luterbacher, JS or send Email.. Product Details of 103-26-4

Authors Komarova, AO; Dick, GR; Luterbacher, JS in ROYAL SOC CHEMISTRY published article about SELECTIVE HYDROGENATION; SOLVATOCHROMIC PARAMETERS; SUSTAINABLE SOLVENTS; MENSHUTKIN REACTION; CINNAMALDEHYDE; GREEN; BIO; FORMALDEHYDE; PERSPECTIVE; CATALYSTS in [Komarova, Anastasia O.; Dick, Graham R.; Luterbacher, Jeremy S.] Ecole Polytech Fed Lausanne EPFL, Inst Chem Sci & Engn, Lab Sustainable & Catalyt Proc, Stn 6, CH-1015 Lausanne, Switzerland; [Dick, Graham R.] Lygg Corp, 2627 Hanover St, Palo Alto, CA 94304 USA in 2021.0, Cited 57.0. 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

Demand for sustainable polar aprotic solvents is increasing due to their unique solubilizing properties and the toxicity of conventional analogs, which are facing pressure from extensive safety legislation. Polar aprotic solvents are particularly difficult to produce renewably because polar molecules that lack hydroxyl groups are rarely found in abundance in the natural world. Here, we explore the use of diformylxylose (DFX), a xylose-derived molecule that can be produced in a single step from lignocellulosic biomass, as a novel polar aprotic bio-based solvent. We notably demonstrate that diformylxylose shows a similar performance to conventional polar aprotic solvents (DMF, NMP, DMSO) in alkylation, cross-coupling (Heck), and hydrogenation reactions. We also demonstrate its straightforward production from commercial xylose and show that it is non-mutagenic, according to the Ames test. Renewable DFX appears to be a greener alternative to common polar aprotic solvents that are considered problematic for industry.

Welcome to talk about 103-26-4, If you have any questions, you can contact Komarova, AO; Dick, GR; Luterbacher, JS or send Email.. 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

Our Top Choice Compound: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.. Application In Synthesis of Methyl 3-phenyl-2-propenoate

Application In Synthesis of Methyl 3-phenyl-2-propenoate. Recently I am researching about WATER-GAS SHIFT; ACID-CATALYZED DEPOLYMERIZATION; ANISOLE DECOMPOSITION; RHODIUM; ALKYLATION; MECHANISM; HYDROGENOLYSIS; TRANSFORMATION; ETHYLTOLUENE; EFFICIENT, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21871277, 21703258]; Beijing Municipal Science & Technology CommissionBeijing Municipal Science & Technology Commission [Z1811000042180042]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Shen, XJ; Meng, M; Mei, QQ; Xiang, JF; Liu, HZ; Han, BX. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

4-Ethyltoluene is a very valuable chemical that is currently produced from fossil feedstocks. Production of 4-ethyltoluene from renewable and cheap lignin is of great significance. Herein, we report a new route to produce 4-ethyltoluene from lignin. It was discovered that RhCl3-LiI-LiBF4 was an efficient catalytic system for the reaction of lignin with CO to form 4-ethyltoluene. In the reaction, ethylbenzene was first formed via demethoxylation and depolymerization of lignin, which was further transformed into 4-ethyltoluene by methylation using methoxy from the lignin. The yield of 4-ethyltoluene could reach 9.5 wt% when GVL-lignin was used as the starting material. Interestingly, 5.2 wt% yield of 4-ethyltoluene was obtained when raw poplar was directly used as the starting material. As far as we know, the transformation of lignin with 4-ethyltoluene as the major product has not been reported. This work provides a new strategy to produce valuable aromatic compounds from renewable resources.

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.. 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

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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.. Product Details of 103-26-4

In 2019 PHYTOCHEMISTRY published article about ESSENTIAL OIL COMPOSITION; BIOCHEMICAL-CHARACTERIZATION; CARBOXYL METHYLTRANSFERASE; ARABIDOPSIS-THALIANA; TERPENE SYNTHASES; INDOLE-3-ACETIC-ACID METHYLTRANSFERASE; SABATH METHYLTRANSFERASES; MOLECULAR-CLONING; VOLATILE; SALICYLATE in [Zhang, Chi; Chen, Xinlu; Chen, Feng] Univ Tennessee, Dept Plant Sci, Knoxville, TN 37996 USA; [Crandall-Stoder, Barbara] Southern Illinois Univ, Dept Plant Biol, Carbondale, IL 62901 USA; [Qian, Ping] Shandong Agr Univ, Chem & Mat Sci Fac, Tai An 271018, Shandong, Peoples R China; [Koellner, Tobias G.] Max Planck Inst Chem Ecol, Dept Biochem, Hans Knoll Str 8, D-07745 Jena, Germany; [Guo, Hong] Univ Tennessee, Dept Biochem Cellular & Mol Biol, Knoxville, TN 37996 USA; [Guo, Hong] Oak Ridge Natl Lab, UT ORNL Ctr Mol Biophys, Oak Ridge, TN 37830 USA in 2019, Cited 63. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Product Details of 103-26-4

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.. 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

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Welcome to talk about 103-26-4, If you have any questions, you can contact Iakovenko, R; Hlavac, J or send Email.. COA of Formula: C10H10O2

Recently I am researching about HYDROGEN/DEUTERIUM EXCHANGE; 3+2 ANNULATION; ALKENES; VINYL; ACTIVATION; REDUCTION; PALLADIUM; DEUTERIUM; OLEFINS; ARYL, Saw an article supported by the Czech Ministry of Education, Youth, and SportsMinistry of Education, Youth & Sports – Czech Republic [IGA_PrF_2020_012]. COA of Formula: C10H10O2. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Iakovenko, R; Hlavac, J. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

Various bromophenylalkenes were reductively photodebrominated by using 1,3-dimethyl-2-phenyl-1H-benzo-[d]imidazoline (DMBI) and 9,10-dicyanoanthracene. With deuterated DMBI analogs (the most effective was DMBI-d(11)), satisfactory to excellent isotopic yields were obtained. DMBI-d(11) could also be regenerated from the reaction mixtures with a recovery rate of up to 50%. The combination of the photodebromination reaction with conventional methods for bromoalkene synthesis enables sequential monodeuteration of a double bond without the necessity of a metal catalyst.

Welcome to talk about 103-26-4, If you have any questions, you can contact Iakovenko, R; Hlavac, J 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

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Welcome to talk about 103-26-4, If you have any questions, you can contact Fischer, O; Heinrich, MR or send Email.. Recommanded Product: Methyl 3-phenyl-2-propenoate

Recommanded Product: Methyl 3-phenyl-2-propenoate. Authors Fischer, O; Heinrich, MR in WILEY-V C H VERLAG GMBH published article about in [Fischer, Oliver; Heinrich, Markus R.] Friedrich Alexander Univ Erlangen Nurnberg, Dept Chem & Pharm, Pharmaceut Chem, Nikolaus Fiebiger Str 10, D-91058 Erlangen, Germany in 2021.0, Cited 87.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

As a novel Sanger-type reagent, 2-fluoro-5-nitrophenyldiazonium tetrafluoroborate enabled the versatile functionalization of primary and secondary aliphatic alcohols. Based on a mild nucleophilic aromatic substitution of the fluorine atom under unprecedented, base-free conditions, the diazonium unit on the aromatic core of the resulting aryl-alkyl ether could be employed for such diverse transformations as radical C-H activation and cyclization, as well as palladium catalyzed cross-coupling reactions.

Welcome to talk about 103-26-4, If you have any questions, you can contact Fischer, O; Heinrich, MR or send Email.. Recommanded Product: 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

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Quality Control of Methyl 3-phenyl-2-propenoate. 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.

Recently I am researching about REUSABLE HETEROGENEOUS CATALYST; SUZUKI-MIYAURA; HIGHLY EFFICIENT; RECYCLABLE CATALYST; MIZOROKI-HECK; RECOVERABLE NANOCATALYST; PD NANOPARTICLES; COMPLEX; SILICA; OXIDATION, Saw an article supported by the Ilam University; Iran National Science Foundation (INSF)Iran National Science Foundation (INSF). Quality Control of Methyl 3-phenyl-2-propenoate. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Tahmasbi, B; Ghorbani-Choghamarani, A. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

In this study, the surface of magnetic MCM-41 nanoparticles (MCM-41/Fe3O4) was modified by 3-aminopropyltriethoxysilane (APTES) and further, 1-methyl imidazole was anchored on their surface using cyanuric chloride as a linker. Then, Pd2+ ions were immobilized on the surface of the modified MCM-41/Fe3O4 (Pd-imi-CC@MCM-41/Fe3O4), and its application was studied as a magnetically recyclable nanocatalyst in carbon-carbon coupling reactions between a wide range of aryl halides and butyl acrylate, methyl acrylate, acrylonitrile, phenylboronic acid, or 3,4-difluorophenylboronic acid under the conditions of a phosphine-free ligand and an air atmosphere. This catalyst has the advantages of both the Fe3O4 nanoparticles and mesoporous MCM-41. The structure of the catalyst was characterized via TEM, SEM, EDS, WDX, N-2 adsorption-desorption isotherm, XRD, TGA, FT-IR, and AAS. Also, the recovered catalyst was characterized via SEM, AAS and FT-IR. All the products from the carbon-carbon coupling reaction were obtained with excellent yields and high TON and TOF values, which indicate the high efficiency and activity of this catalyst. The selectivity of this catalyst was studied with various aryl halides bearing different functional groups. Furthermore, the heterogeneity and stability of Pd-imi-CC@MCM-41/Fe3O4 was studied via AAS, and leaching and poisoning tests. According to the results, this heterogeneous catalyst can be reused several times.

Quality Control of Methyl 3-phenyl-2-propenoate. 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

The Absolute Best Science Experiment for C10H10O2

Welcome to talk about 103-26-4, If you have any questions, you can contact Zhou, CQ; Li, CZ; Siva, S; Cui, HY; Lin, L or send Email.. Quality Control of Methyl 3-phenyl-2-propenoate

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. 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

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.

Welcome to talk about 103-26-4, If you have any questions, you can contact Zhou, CQ; Li, CZ; Siva, S; Cui, HY; Lin, L or send Email.. Quality Control 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

Why do aromatic interactions matter of compound:Methyl 3-phenyl-2-propenoate

Category: esters-buliding-blocks. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Gong, WC; Xu, SJ; Liu, YH; Wang, CM; Martin, K; Meng, LZ or concate me.

An article Chemical composition of floral scents from three Plumeria rubra L. (Apocynaceae) forms linked to petal color proprieties WOS:000472124800011 published article about FLOWER COLOR; POLLINATION SYNDROMES; GAS-CHROMATOGRAPHY; DECEPTIVE ORCHID; FRAGRANCE; SELECTION; BIOCHEMISTRY; POLYMORPHISM; POPULATION; CHEMISTRY in [Gong, Wei-Chang; Xu, Shi-Juan; Liu, Yan-Hong; Wang, Chuan-Ming; Meng, Ling-Zeng] Honghe Univ, Coll Life Sci & Technol, Xuefu Rd, Mengzi 661199, Yunnan, Peoples R China; [Meng, Ling-Zeng] Chinese Acad Sci, Xishuangbanna Trop Bot Garden, Mengla 666303, Yunnan, Peoples R China; [Martin, Konrad; Meng, Ling-Zeng] Univ Hohenheim, Inst Agr Sci Trop, Hans Ruthenberg Inst, 490f, D-70593 Stuttgart, Germany in 2019.0, Cited 51.0. Category: esters-buliding-blocks. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

The floral scents of three forms of cultivated Plumeria rubra L. were evaluated through mass flowering phenology using the dynamic headspace adsorption method and were identified with coupled gas chromatography and mass spectrometry. The forms P. rubra f. acutifolia and P. rubra f. lutea had white and yellow flower petals, respectively, and the flower petals of P. rubra f. rubra were red. Although 68 components of the flower scents of the three forms were recorded in different proportions, only 14 chemical compounds were identified with statistically significance. The main volatile compounds in the red form of P. rubra L. were fatty acid derivatives (56.75%). The main compounds in the white and yellow forms of P. rubra L. were benzenoid and terpene, with proportions of 48.38% and 33.33% in P. rubra f. acutifolia and proportions of 42.30% and 47.43% in P. rubra f. lutea, respectively. These differences in the flower scents might be one result of the minor genetic differences between these forms, similar to the role of genetic differences in the flower color combinations of the three forms. We conclude that petal color traits can, to some extent, reflect differences in floral scent compositions and that minor genetic differences of different plant forms exert impacts not only on flower color but also on the phytochemistry of floral scents.

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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