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Carbamic acid, [(4-hydroxyphenyl)iminomethyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76223-53-5

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76223-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76223-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76223-53:
(7*7)+(6*6)+(5*2)+(4*2)+(3*3)+(2*5)+(1*3)=125
125 % 10 = 5
So 76223-53-5 is a valid CAS Registry Number.

76223-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[(4-hydroxyanilino)methylidene]carbamate

1.2 Other means of identification

Product number -
Other names N-benzyloxycarbonyl-p-amidinophenol

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:76223-53-5 SDS

76223-53-5Relevant academic research and scientific papers

INVERSE SUBSTRATES IX. AMIDINOPHENYL ESTERS DERIVED FROM AMINO ACIDS AND PEPTIDES : SYNTHESIS AND PROPERTIES AS TRYPSIN SUBSTRATES

Fujioka, Toshiyuki,Tanizawa, Kazutaka,Nakayama, Hitoshi,Kanaoka, Yuichi

, p. 1899 - 1905 (2007/10/02)

Methods for preparation of p-amidinophenyl esters from amino acid derivatives are described.Blocking of the amidino function with the benzyloxycarbonyl group and its deblocking by catalytic hydrogenation after coupling were satisfactory. p-Amidino-phenyl esters are of special interest because of their susceptibility to the hydrolytic enzyme, trypsin, and some parameters of the hydrolysis of these compounds by tripsin are presented.Keywords - p-amidinophenyl ester; synthetic substrates; ester formation; trypsin; enzyme kinetics; deacylation rate constant

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