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2-Propenoic acid, 3-chloro-3-phenyl-, methyl ester, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56377-29-8

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56377-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56377-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,7 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56377-29:
(7*5)+(6*6)+(5*3)+(4*7)+(3*7)+(2*2)+(1*9)=148
148 % 10 = 8
So 56377-29-8 is a valid CAS Registry Number.

56377-29-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-chloro-3-phenylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 3-chloro-3-phenyl-2-propenoic acid,methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56377-29-8 SDS

56377-29-8Relevant academic research and scientific papers

Palladium-catalysed annulation of β-chloro-α,β-unsaturated esters with internal alkynes leading to 2H-pyran-2-ones

Hua,Tanaka

, p. 179 - 184 (2001)

Heteroannulation of β-chloro-α,β-unsaturated esters with internal alkynes proceeded in the presence of triethylamine and palladium complexes, bis(triphenylphosphine)palladium species in particular, to afford to 2H-pyran-2-ones. Treatment of methyl (Z)-3-c

One-pot tandem hydrophenylation and ionic hydrogenation of 3-phenylpropynoic acid derivatives under superelectrophilic activation

Nilov, Denis I.,Vasilyev, Aleksander V.

, p. 5714 - 5717 (2015/09/29)

The reactions of esters and amides of 3-phenylpropynoic acid with strong Lewis acids AlX3 (X = Cl, Br) or conjugate Br?nsted-Lewis superacids HX-AlX3 (X = Cl, Br) in benzene and cyclohexane at room temperature afforded 3,3-diphenylpropanoic acid derivatives in up to 94% yield. This tandem reaction of the acetylene bond proceeded by hydrophenylation followed by ionic hydrogenation.

Chloroesterification of enynes catalyzed by NHC rhodium compounds

Ji, Young Baek,Sang, Ick Lee,So, Hee Sim,Young, Keun Chung

, p. 551 - 554 (2008/12/21)

An efficient rhodium N-heterocyclic carbene (NHC)-catalyzed chloroesterification of terminal alkynes and enynes has been developed. The reaction was highly regio- and stereospecific: the Z-isomer was obtained as the sole product. Georg Thieme Verlag Stutt

General and selective synthesis of (Z)-3-haloacrylates via palladium-catalyzed carbonylation of terminal alkynes

Li, Jin-Heng,Tang, Shi,Xie, Ye-Xiang

, p. 477 - 479 (2007/10/03)

(Chemical Equation Presented) A general and selective palladium-catalyzed carbonylation of terminal alkynes method for the synthesis of (Z)-3-haloacrylates is presented. In the presence of a catalytic amount of PdX2 and 5 equiv of CuX2/su

Novel stereospecific synthesis of 3-chloroacrylate esters via palladium- catalyzed carbonylation of terminal acetylenes

Li, Jinheng,Jiang, Huanfeng,Feng, Aiqun,Jia, Lanqi

, p. 5984 - 5987 (2007/10/03)

A simple and effective method for the highly regio- and stereospecific synthesis of (Z)-3-chloroacrylate esters is described. Using terminal acetylenes and primary, secondary, and tertiary aliphatic alcohols as substrates, the carbonylation reactions were

ELECTROCHEMICAL CROSS-COUPLING OF ORGANIC HALIDES: TRICHLORMETHYLATION AND RELATED SYNTHESIS OF GEM-DICHLORO COMPOUNDS

Nedelec, J. Y.,Ait-Haddou-Mouloud, H.,Folest, J. C.,Perichon, J.

, p. 1699 - 1700 (2007/10/02)

The cross-coupling of activated alkyl halides with carbon tetrachloride or substituted trichloromethanes can be obtained electrochemically in good yield in an undivided cell with a sacrificial anode.

Electrochemical Cross-Coupling of Alkyl Halides in the Presence of a Sacrificial Anode

Nedelec, Jean-Yves,Mouloud, Hassan Ait Haddou,Folest, Jean-Claude,Perichon, Jacques

, p. 4720 - 4724 (2007/10/02)

The electrochemical trichloromethylation of various alkyl halides has been obtained in high yields in an undivided cell in the presence of a sacrificial anode.This cross-coupling process has been extended to the preparation of numerous gem-dichloro compounds from trichloro-substituted methanes and alkyl halides.Zinc,magnesium or aluminium were used as anodes according to the reduction potentiel of the reagents.Mixtures of polar aprotic solvents,e.g.THF-TMU or THF-NMP, were found more appropriate than pure solvents.The critical role of the metallic ions from the consumption of the anode has been clearly evidenced.

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