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Methyl 3-(benzylcarbaMoyl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

925159-45-1

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925159-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 925159-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,1,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 925159-45:
(8*9)+(7*2)+(6*5)+(5*1)+(4*5)+(3*9)+(2*4)+(1*5)=181
181 % 10 = 1
So 925159-45-1 is a valid CAS Registry Number.

925159-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-(benzylcarbamoyl)benzoate

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:925159-45-1 SDS

925159-45-1Relevant academic research and scientific papers

Discovery of the first histone deacetylase 6/8 dual inhibitors

Olson, David E.,Wagner, Florence F.,Kaya, Taner,Gale, Jennifer P.,Aidoud, Nadia,Davoine, Emeline L.,Lazzaro, Fanny,We?wer, Michel,Zhang, Yan-Ling,Holson, Edward B.

, p. 4816 - 4820 (2013/07/19)

We disclose the first small molecule histone deacetylase (HDAC) inhibitor (3, BRD73954) capable of potently and selectively inhibiting both HDAC6 and HDAC8 despite the fact that these isoforms belong to distinct phylogenetic classes within the HDAC family of enzymes. Our data demonstrate that meta substituents of phenyl hydroxamic acids are readily accommodated upon binding to HDAC6 and, furthermore, are necessary for the potent inhibition of HDAC8.

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