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2-Propenoic acid, 2-(benzoylamino)-3-(4-chlorophenyl)-, methyl ester, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82301-66-4

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82301-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82301-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,0 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82301-66:
(7*8)+(6*2)+(5*3)+(4*0)+(3*1)+(2*6)+(1*6)=104
104 % 10 = 4
So 82301-66-4 is a valid CAS Registry Number.

82301-66-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-N-benzoylamino-3-(4-chlorophenyl) acrylic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl Z-2-benzamido-3-p-chlorophenyl-2-propenoate

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:82301-66-4 SDS

82301-66-4Relevant academic research and scientific papers

Reactivity of unsaturated 5(4H)-oxazolones with Hg(II) acetate: Synthesis of methyl N-benzoylamino-3-arylacrylates

Roiban, Gheorghe-Doru,Soler, Tatiana,Contel, Maria,Grosu, Ion,Cativiela, Carlos,Urriolabeitia, Esteban P.

experimental part, p. 195 - 203 (2011/10/31)

An efficient and high-yield procedure to prepare methyl N-benzoylamino-3-arylacrylates from unsaturated (Z)-2-aryl-4-arylidene-5-(4H)- oxazolones and Hg(OAc)2 in methanol is described herein. The observed reactivity of mercury(II) acetate here

The use of cyclohexyl isocyanide in the esterification of N-benzoyl α-amino acids derivatives

Hassanabadi, Alireza,Anary-Abbasinejad, Mohammad,Niri, Atefeh Ahmadi,Feizpoor, Rozita

, p. 468 - 470 (2011/11/29)

The N-benzoyl of α,β-dehydroamino acids that were obtained by condensation of N-benzoylglycine and an aldehyde, were esterified with an alcohol in high yield using cyclohexyl isocyanide to activate the carboxylic acid under neutral conditions.

One-pot process to Z-α-benzoylamino-acrylic acid methyl esters via potassium phosphate-catalyzed Erlenmeyer reaction

Cleary, Thomas,Brice, Jodie,Kennedy, Nicole,Chavez, Flavio

supporting information; experimental part, p. 625 - 628 (2010/04/05)

A practical and efficient two reaction sequence one-pot process for the synthesis of Z-α-benzoylamino-acrylic acid methyl esters was developed. The process involves a potassium phosphate-catalyzed Erlenmeyer reaction of aromatic aldehydes with hippuric acid followed by an oxazolone ring-opening methanolysis. This process afforded a good overall yield and an excellent product quality via a simple workup.

An usual behaviour of ethers in presence of azlactones under ultrasound irradiation to give esters

Rajaram, S.,Lalitha, N.,Iyengar, D. S.

, p. 761 - 763 (2007/10/03)

The phenomenon of ester formation from ethers and azlactones under sonolysis has been observed.

A new methodology for the synthesis of N-acylaminocinnamates

Rao, Ch. Chennakesava,Lalitha, Nagubandi

, p. 3 (2007/10/02)

A new synthesis of biologically active N-protected amino acids (2) and amides (4) from 4-ylidene-5(4H)-oxazolones (1) is described.

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