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4-Pyrimidinemethanol, a-(2-fluorophenyl)-2-(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918870-23-2

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918870-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918870-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,8,7 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 918870-23:
(8*9)+(7*1)+(6*8)+(5*8)+(4*7)+(3*0)+(2*2)+(1*3)=202
202 % 10 = 2
So 918870-23-2 is a valid CAS Registry Number.

918870-23-2SDS

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 (2-fluorophenyl)(2-(methylthio)pyrimidin-4-yl)methanol

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:918870-23-2 SDS

918870-23-2Relevant academic research and scientific papers

The development of 2-benzimidazole substituted pyrimidine based inhibitors of lymphocyte specific kinase (Lck)

Sabat, Mark,VanRens, John C.,Laufersweiler, Matthew J.,Brugel, Todd A.,Maier, Jennifer,Golebiowski, Adam,De, Biswanath,Easwaran, Vijayasurian,Hsieh, Lily C.,Walter, Richard L.,Mekel, Marlene J.,Evdokimov, Artem,Janusz, Michael J.

, p. 5973 - 5977 (2007/10/03)

This communication details the synthesis, biological activity, and binding mode of a novel class of 2-benzimidazole substituted pyrimidines. The most potent analogs disclosed showed low nanomolar activity for the inhibition of Lck kinase and a representat

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