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42288-55-1

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42288-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42288-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,8 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42288-55:
(7*4)+(6*2)+(5*2)+(4*8)+(3*8)+(2*5)+(1*5)=121
121 % 10 = 1
So 42288-55-1 is a valid CAS Registry Number.

42288-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-aminomethyl-phenyl)-acetic acid , hydrochloride

1.2 Other means of identification

Product number -
Other names 3-aminomethylphenylacetic acid hydrochloride

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:42288-55-1 SDS

42288-55-1Relevant articles and documents

Synthesis and evaluation of novel aromatic substrates and competitive inhibitors of GABA aminotransferase

Clift, Michael D.,Silverman, Richard B.

, p. 3122 - 3125 (2008/12/22)

The design, synthesis, and evaluation of novel γ-aminobutyric acid aminotransferase (GABA-AT) inhibitors and inactivators can lead to the discovery of new GABA-related therapeutics. To this end, a series of aromatic amino acid compounds was synthesized to aid in the design of new inhibitors and inactivators of GABA-AT. All compounds were tested as competitive inhibitors of GABA-AT. The amino acids with benzylic amines were also tested as substrates for GABA-AT. It was found that these compounds were all poor competitive inhibitors of GABA-AT, but some were substrates of the enzyme, suggesting their utility as scaffolds for potential GABA-AT mechanism-based inactivators. Computer modeling was used to rationalize the substrate activity of the various compounds.

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