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696-80-0

696-80-0

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696-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 696-80-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 696-80:
(5*6)+(4*9)+(3*6)+(2*8)+(1*0)=100
100 % 10 = 0
So 696-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H4F2N2/c1-3-2-4(6)9-5(7)8-3/h2H,1H3

696-80-0SDS

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 2,4-difluoro-6-methylpyrimidine

1.2 Other means of identification

Product number -
Other names Pyrimidine,2,4-difluoro-6-methyl

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:696-80-0 SDS

696-80-0Relevant articles and documents

PYRIMIDINE DERIVATIVES USED AS ITK INHIBITORS

-

Page/Page column 132, (2010/10/03)

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular ltk activity.

Fluorinated Heterocyclic Compounds. 2. 2,4-Difluoro and 4-Amino-2-fluoropyrimidines, Nucleoside Base Analogs

Svirskaya, Polina I.,Yedidia, Varda,Leznoff, Clifford C.,Miller, Jack M.

, p. 149 - 153 (2007/10/02)

Nucleoside base analogs in which fluoro substituents replace the enolic hydroxy groups of uracil, thymine and cytosine have been prepared.Improved methods for the preparation and isolation of the known 2,4-difluoropyrimidine, 2,4-difluoro-6-methylpyrimidine and the new 2,4-difluoro-5-methylpyrimidine, 2-fluoro-4-aminopyrimidine, 4-fluoro-2-aminopyrimidine, and other alkylaminofluoropyrimidines are described.

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