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(S)-2-Benzyloxycarbonylamino-3-(4-carbamoyl-phenyl)-propionic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

223593-01-9

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223593-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223593-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,5,9 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 223593-01:
(8*2)+(7*2)+(6*3)+(5*5)+(4*9)+(3*3)+(2*0)+(1*1)=119
119 % 10 = 9
So 223593-01-9 is a valid CAS Registry Number.

223593-01-9SDS

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 benzyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-carbamoylphenyl)propanoate

1.2 Other means of identification

Product number -
Other names -

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:223593-01-9 SDS

223593-01-9Relevant academic research and scientific papers

A selective method for the preparation of primary amides: Synthesis of Fmoc-L-4 carboxamidophenylalanine and other compounds

Wang, Wei,McMurray, John S.

, p. 2501 - 2504 (1999)

A new method for the synthesis of primary amides was developed in which carboxylic acids were treated with ammonium chloride in the presence of peptide synthesis coupling agents and base at room temperature. These mild conditions allow the conversion of carboxyl groups to primary amides on substrates possessing sensitive functional groups such as esters and the base-labile Fmoc protecting group.

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