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Carbamic acid, [(phenylamino)carbonyl]-, 3-chlorophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87343-75-7

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87343-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87343-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,4 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87343-75:
(7*8)+(6*7)+(5*3)+(4*4)+(3*3)+(2*7)+(1*5)=157
157 % 10 = 7
So 87343-75-7 is a valid CAS Registry Number.

87343-75-7SDS

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 4-phenyl-allophanic acid-(3-chloro-phenyl ester)

1.2 Other means of identification

Product number -
Other names 4-Phenyl-allophansaeure-(3-chlor-phenylester)

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:87343-75-7 SDS

87343-75-7Relevant academic research and scientific papers

Nouvelles syntheses de phenyl-4 allophanates

Al Sabbagh, Mohamed Mowafak,Calmon, Michelle,Calmon, Jean-Pierre

, p. 73 - 77 (2007/10/02)

The synthesis of eighteen alkyl or phenyl 4-phenylallophanates is described.The classical methods used for the preparation of allophanates - namely, condensation between an isocyanate and a carbamate, reaction between a urea and a carbonate, desulphurization of 3-thioallophanic acid esters - proved to be unsuitable for the synthesis of 4-phenylallophanic acid phenyl esters.Variously substituted 4-phenylallophanates can be obtained by reacting a chloroformate with a phenylurea in the presence of pyridine, which promotes the transfer of the carboxylate group.The occurence of electrondonating substituents, such as CH3, at the nitrogen atom receiving the carboxylate group promotes the reaction.The low yields observed for aliphatic esters can be accounted for by the instability of the alkyl chloroformate-pyridine complex.The structures of the derivatives synthesized was corroborated by the analysis of their n.m.r. and u.v. spectra. Non-commercial phenyl chloroformates were prepared by reacting phosgene with a sodium phenolate in the presence of anhydrous benzene.

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