Category: 103-26-4

An article Regioselective Radical Borylation of alpha,beta-Unsaturated Esters and Related Compounds by Visible Light Irradiation with an Organic Photocatalyst WOS:000661126700051 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. Application In Synthesis 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).

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.. 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

I found the field of Biochemistry & Molecular Biology; Chemistry; Polymer Science very interesting. Saw the article Controlled Radical Copolymerization of Cinnamic Derivatives as Renewable Vinyl Monomers with Both Acrylic and Styrenic Substituents: Reactivity, Regioselectivity, Properties, and Functions published in 2019.0. SDS of cas: 103-26-4, Reprint Addresses Satoh, K; Kamigaito, M (corresponding author), Nagoya Univ, Grad Sch Engn, Dept Mol & Macromol Chem, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan.. The CAS is 103-26-4. Through research, I have a further understanding and discovery 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.

Welcome to talk about 103-26-4, If you have any questions, you can contact Terao, Y; Satoh, K; Kamigaito, M or send Email.. 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

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. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Name: Methyl 3-phenyl-2-propenoate

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.

Name: 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

An article Heterogeneous Organo- and Metal Catalysis Using Phosphine Oxide Derivatives Anchored on Multiwalled Carbon Nanotubes WOS:000579231800001 published article about KINETIC RESOLUTION; FUNCTIONALIZATION; NANOCARBONS; DIAZONIUM in [Ligi, Maria Cristina; Biagiotti, Giacomo; Cicchi, Stefano] Univ Firenze, Dept Chem, Via Lastruccia 3-13, I-50019 Florence, Italy; [Flis, Anna; Michal Pietrusiewicz, K.] Marie Curie Sklodowska Univ, Dept Organ Chem, Ul Gliniana 33, PL-20614 Lublin, Poland; [Biagiotti, Giacomo; Serrano, Giulia; Cicchi, Stefano] INSTM Natl Interuniv Consortium Mat Sci & Technol, Via G Giusti 9, I-50121 Florence, Italy; [Serrano, Giulia] Univ Firenze, Dept Ind Engn, Via S Marta 3, I-50139 Florence, Italy; [Cicchi, Stefano] CNR, Inst Chem Organometall Cpds ICCOM, Via Madonna Piano 10, I-50019 Sesto Fiorentino, Italy in 2020.0, Cited 36.0. 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

Oxidized multiwalled carbon nanotubes were modified anchoring phosphine oxides and used as heterogeneous catalysts. A proper substitution of the phosphine oxides allowed the use of the Tour reaction and the nitrene cycloaddition to obtain functionalized carbon nanotubes (CNT) with a loading up to 0.73 mmol/g of material. The catalysts proved efficient in Wittig reactions, Mitsunobu reactions, and Staudinger ligations. Furthermore, the phosphorus decorated CNT were used to produce nanocomposite with Pd nanoparticles able to catalyze Heck reactions.

Welcome to talk about 103-26-4, If you have any questions, you can contact Ligi, MC; Flis, A; Biagiotti, G; Serrano, G; Pietrusiewicz, KM; Cicchi, S or send Email.. Computed Properties of 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 Moradi, R; Ziarani, GM; Badiei, A; Mohajer, F in WILEY published article about METAL-CATALYSTS; ARYL CHLORIDES; OPTICAL SENSOR; NANOPARTICLES; SILICAS; OLEFINS; HYBRID; ACTIVATION; MECHANISM; ARYLATION in [Moradi, Razieh; Mohammadi Ziarani, Ghodsi; Mohajer, Fatemeh] Alzahra Univ, Dept Chem, Vanak Sq,POB 1993893973, Tehran, Iran; [Badiei, Alireza] Univ Tehran, Sch Chem, Coll Sci, Tehran, Iran in 2020.0, Cited 57.0. 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

In the present study, the modification of a mesoporous organosilica nanocomposite SBA-15 (Santa Barbara Amorphous 15) was carried out in two steps, first through the surface functionalization of SBA-Pr-NH(2)with 2-chloroquinoline-3-carbaldehyde to form SBA-Pr-NCQ, and then through a post-modification process with palladium ions. The target nanocompound structure of SBA-Pr-NCQ-Pd was characterized by different techniques (thermogravimetric analysis, X-ray diffraction, scanning electron microscopy, Energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy). The catalytic performance of the porous inorganic-organic hybrid nanocomposite (SBA-Pr-NCQ-Pd) in one of the most important carbon-carbon bond-forming processes, the Mizoroki-Heck coupling reaction of aryl halides and methacrylate in water/ethanol media, was examined. Compared to previous reports, this protocol afforded some advantages, such as high yields of products, short reaction times, catalyst stability without leaching, simple methodology, easy workup, and greener conditions. Also, the nanocatalyst can be easily separated from the reaction mixture and reused several times without a significant decrease in activity and promises economic as well as environmental benefits.

Welcome to talk about 103-26-4, If you have any questions, you can contact Moradi, R; Ziarani, GM; Badiei, A; Mohajer, 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

Safety of Methyl 3-phenyl-2-propenoate. In 2019.0 PHYS CHEM CHEM PHYS published article about PHOTOACTIVE YELLOW PROTEIN; CLUSTER-EXPANSION; EXCITED-STATES; WAVE-FUNCTION; ECTOTHIORHODOSPIRA-HALOPHILA; HYDRATED COMPLEX; METHYL CINNAMATE; SINAPIC ACID; DYNAMICS; SAC in [Kinoshita, Shin-nosuke; Inokuchi, Yoshiya; Onitsuka, Yuuki; Kohguchi, Hiroshi; Ebata, Takayuki] Hiroshima Univ, Grad Sch Sci, Dept Chem, Higashihiroshima 7398526, Japan; [Akai, Nobuyuki] Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn BASE, Naka Cho, Koganei, Tokyo 1848588, Japan; [Shiraogawa, Takafumi; Ehara, Masahiro] SOKENDAI, Grad Univ Adv Studies, Okazaki, Aichi 4448585, Japan; [Ehara, Masahiro] Inst Mol Sci & Res Ctr Computat Sci, 38 Myodayi, Okazaki, Aichi 4448585, Japan; [Yamazaki, Kaoru] Tohoku Univ, Inst Mat Res, Aoba Ku, Katahira 2-1-1, Sendai, Miyagi 9808577, Japan; [Harabuchi, Yu; Maeda, Satoshi] Hokkaido Univ, Fac Sci, Dept Chem, Sapporo, Hokkaido 0600810, Japan; [Harabuchi, Yu] JST, PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan; [Harabuchi, Yu; Maeda, Satoshi] Hokkaido Univ, Inst Chem React Design & Discovery WPI ICReDD, Sapporo, Hokkaido 0010021, Japan in 2019.0, Cited 56.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

The electronic states and photochemistry including nonradiative decay (NRD) and trans(E) -> cis(Z) isomerization of methylcinnamate (MC) and its hydrogen-bonded complex with methanol have been investigated under jet-cooled conditions. S-1((1)n pi*) and S-2((1)pi pi*) are directly observed in MC. This is the first direct observation of S-1(1n pi*) in cinnamate derivatives. Surprisingly, the order of the energies between the n pi* and pi pi* states is opposite to substituted cinnamates. TD-DFT and SAC-CI calculations support the observed result and show that the substitution to the benzene ring largely lowers the (1)pi pi* energy while the effect on (1)n pi* is rather small. The S-2(pi pi*) state lifetime of MC is determined to be equal to or shorter than 10 ps, and the production of the transient T-1 state is observed. The T-1(pi pi*) state is calculated to have a structure in which propenyl C=C is twisted by 90 degrees, suggesting the trans -> cis isomerization proceeds via T-1. The production of the cis isomer is confirmed by low-temperature matrix-isolated FTIR spectroscopy. The effect of H-bonding is examined for the MC-methanol complex. The S-2 lifetime of MC-methanol is determined to be 180 ps, indicating that the H-bonding to the C=O group largely prohibits the (1)pi pi* -> (1)n pi* internal conversion. This lifetime elongation in the methanol complex also describes well a higher fluorescence quantum yield of MC in methanol solution than in cyclohexane, while such a solvent dependence is not observed in para-substituted MC. Determination of the photochemical reaction pathways of MC and MC-methanol will help us to design photofunctional cinnamate derivatives.

Safety 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

Quality Control of Methyl 3-phenyl-2-propenoate. Recently I am researching about ESSENTIAL OIL COMPOSITION; BASILICUM L.; INTERSPECIFIC HYBRIDS; DNA BARCODES; FUNCTIONAL-CHARACTERIZATION; MOLECULAR CHARACTERIZATION; ISSR MARKERS; IDENTIFICATION; DIVERSITY; SYNTHASE, Saw an article supported by the University Grants Commission (UGC, New Delhi, India)University Grants Commission, India; CSIR-NCL-IGIB Joint Research Initiative program [BSC0124]. Published in ELSEVIER in AMSTERDAM ,Authors: Gurav, TP; Jayaramaiah, RH; Punekar, SA; Dholakia, BB; Giri, AP. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

The genus Ocimum is a boutique of a diverse set of specialized metabolites such as terpenoids and phenylpropanoids. Each Ocimum species and its cultivars represent a characteristic chemical profile. The present study explored the two interspecific Ocimum hybrids originating through a serendipitous natural cross between O. kilimandscharicum and O. basilicum. These two novel Ocimum hybrids exhibited intermediate morphological features of two parental species. Inter simple sequence repeats (ISSR) analysis and DNA barcoding with the plastid non-coding trnH-psbA intergenic spacer region reaffirmed unambiguous parental identification and differentiation of these natural hybrids from other available Ocimum species. Consequently, gas chromatographymass spectrometry-based metabolite profiling of two hybrids identified them as specific chemotypes with the presence of a unique blend of specialized metabolites from the parental species, which are either rich in terpenes or phenylpropanoids. Additionally, expression analysis of key genes from terpenoid and phenylpropanoid pathways corroborated with differential metabolite accumulation. Thus, these two Ocimum hybrids represented the novel chemotypes, which could be useful in commercial cultivation to produce novel essential oil and bioactive constituents. Further, the resulting metabolite diversity could have potential industrial applications in the areas of healthcare, bioremediation, and crop protection.

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

HPLC of Formula: C10H10O2. Recently I am researching about METAL-CATALYSTS; ARYL CHLORIDES; OPTICAL SENSOR; NANOPARTICLES; SILICAS; OLEFINS; HYBRID; ACTIVATION; MECHANISM; ARYLATION, Saw an article supported by the Research Council of Alzahra University; University of TehranUniversity of Tehran. Published in WILEY in HOBOKEN ,Authors: Moradi, R; Ziarani, GM; Badiei, A; Mohajer, F. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

In the present study, the modification of a mesoporous organosilica nanocomposite SBA-15 (Santa Barbara Amorphous 15) was carried out in two steps, first through the surface functionalization of SBA-Pr-NH(2)with 2-chloroquinoline-3-carbaldehyde to form SBA-Pr-NCQ, and then through a post-modification process with palladium ions. The target nanocompound structure of SBA-Pr-NCQ-Pd was characterized by different techniques (thermogravimetric analysis, X-ray diffraction, scanning electron microscopy, Energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy). The catalytic performance of the porous inorganic-organic hybrid nanocomposite (SBA-Pr-NCQ-Pd) in one of the most important carbon-carbon bond-forming processes, the Mizoroki-Heck coupling reaction of aryl halides and methacrylate in water/ethanol media, was examined. Compared to previous reports, this protocol afforded some advantages, such as high yields of products, short reaction times, catalyst stability without leaching, simple methodology, easy workup, and greener conditions. Also, the nanocatalyst can be easily separated from the reaction mixture and reused several times without a significant decrease in activity and promises economic as well as environmental benefits.

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.. HPLC 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

An article Aroma characteristics of Cabernet Sauvignon wines from Loess Plateau in China by QDA (R), Napping (R) and GC-O analysis WOS:000516055900001 published article about VOLATILE COMPOUNDS; WHITE WINES; PROFILE; REGION; ACIDS in [Tang, Ke; Tian, Xin; Ma, Yue; Sun, Yulu; Xu, Yan] Jiangnan Univ, Minist Educ, Key Lab Ind Biotechnol, 1800 Lihu Ave, Wuxi, Jiangsu, Peoples R China; [Tang, Ke; Tian, Xin; Ma, Yue; Sun, Yulu; Xu, Yan] Jiangnan Univ, State Key Lab Food Sci & Technol, 1800 Lihu Ave, Wuxi, Jiangsu, Peoples R China; [Qi, Xinchun; Miu, Chengpeng] Chateau Rongzi Co Ltd, Linfen, Shanxi, Peoples R China in 2020.0, Cited 37.0. Application In Synthesis 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

Loess Plateau is a new rapidly developing wine region in China, but wine style from this region is rarely studied. The aroma typicalies and differences of Cabernet Sauvignon wines between Loess Plateau and other three main regions (Shandong, Ningxia and Xinjiang) in China were comprehensively analyzed by Quantitative Descriptive Analysis (QDA (R)), Napping (R) and Gas Chromatography-Olfactometry (GC-O) analysis. Results showed that differences existed between wines from Loess Plateau and other three regions in China based on their aroma characteristics. The results of QDA (R) and Napping (R) revealed that wines from Loess Plateau had richer fruity aroma, especially the typical hawthorn aroma. A similar result showed that the fruity compounds had higher flavor dilution factors in wines from Loess Plateau by aroma extract dilution analysis. Identified by GC-O and gas chromatography-mass spectrometric, ethyl butanoate, isoamyl formate and butyl acetate were key compounds for the fruity aroma of wines from Loess Plateau.

Application In Synthesis 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

Authors Lu, XP; Liu, JH; Weng, H; Ma, ZQ; Zhang, X in JOHN WILEY & SONS LTD published article about PLANT ESSENTIAL OILS; BOTANICAL INSECTICIDES; FUMIGANT TOXICITY; ONION THRIPS; JOINT ACTION; THYSANOPTERA; MICROEMULSIONS; CONSTITUENTS; NANOEMULSION; COMPONENTS in [Lu, Xiao-Peng; Liu, Jia-Huan; Ma, Zhi-Qing; Zhang, Xing] Northwest A&F Univ, Res & Dev Ctr Biorat Pesticide, Yangling 712100, Shaanxi, Peoples R China; [Weng, Hua] Qinghai Univ, Acad Agr & Forestry Sci, Xining, Qinghai, Peoples R China; [Ma, Zhi-Qing; Zhang, Xing] Res Ctr Biopesticide Technol & Engn, Yangling, Shaanxi, Peoples R China in 2020.0, Cited 51.0. Name: 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

BACKGROUND Thrips Anaphothrips obscurus are one of the cosmopolitan major pests feeding on cereals and other grasses. In order to develop alternatives of chemical insecticides for thrips control, based on fumigant activity screening and evaluation of 22 essential oil (EO) compounds against the thrips, the binary interactions of methyl salicylate and carvacrol (MS-C) with high fumigant toxicity were studied systematically by bioassay and field trials. RESULTS The bioassay results showed that six in 22 EO compounds had high fumigant toxicity against both the second-instar nymphs and adults of A. obscurus, including methyl salicylate, carvacrol, thymol, trans-cinnamaldehyde, diallyl trisulfide, and L-perillaldehyde. Furthermore, the combination of methyl salicylate mixed with carvacrol at a volume ratio of 5:5 exhibited the most significant synergism against A. obscurus, with a poison ratio value of 1.32 and a co-toxicity coefficient of 151.15. The optimal formulation of microemulsion (ME) was composed of 5% methyl salicylate, 5% carvacrol, 46% adjuvant and 44% deionized water. The result of dynamic light scattering and stability showed that MS-C 10% ME was a transparent, single-phase and homogeneous liquid system. Field trials indicated that the ME displayed a significant control efficacy of about 89.17% on thrips in peppers, and 82.59% in broad bean on the seventh day post application with a dosage of 600.0 g A.I hm(-2), respectively. CONCLUSION The binary combination of MS-C possesses strikingly synergistic action against thrips A. obscurus, and the MS-C 10% ME has the potential to be developed as a botanical pesticide product for thrips control. (c) 2019 Society of Chemical Industry

Name: Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Lu, XP; Liu, JH; Weng, H; Ma, ZQ; Zhang, X 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