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N2-ethyl-6-chloro-pyrimidine-2,4-diyldiamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70958-42-8

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70958-42-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70958-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,5 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70958-42:
(7*7)+(6*0)+(5*9)+(4*5)+(3*8)+(2*4)+(1*2)=148
148 % 10 = 8
So 70958-42-8 is a valid CAS Registry Number.

70958-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N2-ethyl-6-chloro-pyrimidine-2,4-diyldiamine

1.2 Other means of identification

Product number -
Other names 6-Chloro-N2-ethyl-pyrimidine-2,4-diamine

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:70958-42-8 SDS

70958-42-8Downstream Products

70958-42-8Relevant academic research and scientific papers

Alpha V integrin receptor antagonists

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, (2008/06/13)

The present invention relates to novel imidazolidinone derivatives thereof, their synthesis, and their use as αv integrin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors αvβ3 and/or

Alpha V integrin receptor antagonists

-

, (2008/06/13)

The present invention relates to novel alkanoic acid derivatives thereof, their synthesis, and their use as αv integrin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors αvβ3 and/or α

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