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157643-41-9

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157643-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157643-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,6,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 157643-41:
(8*1)+(7*5)+(6*7)+(5*6)+(4*4)+(3*3)+(2*4)+(1*1)=149
149 % 10 = 9
So 157643-41-9 is a valid CAS Registry Number.

157643-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-carboxyethyl)aziridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Aziridinepropanoicacid,2-carboxy-,(?A'A A'A currency)

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:157643-41-9 SDS

157643-41-9Upstream product

157643-41-9Downstream Products

157643-41-9Relevant articles and documents

The Synthesis and Stability of Aziridino-glutamate, an Irreversible Inhibitor of Glutamate Racemase

Tanner, Martin E.,Miao, Shichang

, p. 4073 - 4076 (1994)

Aziridino-glutamate (2-(2-carboxyethyl)aziridine-2-carboxylic acid, (+/-)4 was synthesized by heating α-fluoromethylglutamate in base.In neutral solution, 4 was shown to cyclize to the γ-lactone 5 with a half life of 4 minutes.Aziridino-glutamate was shown to irreversibily inactivate glutamate racemase by alkylating an active site cystein residue.Electrospray mass spectrometry was used to establish that a covalent bond had formed and that this bond protects one the enzyme's two cysteine residues from reacting with iodoacetate under denaturing conditions.

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