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Thiazolo[5,4-d]pyrimidin-7-amine, 2-(1-methyl-4-phenyl-1H-imidazol-5-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

655253-60-4

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655253-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 655253-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,5,2,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 655253-60:
(8*6)+(7*5)+(6*5)+(5*2)+(4*5)+(3*3)+(2*6)+(1*0)=164
164 % 10 = 4
So 655253-60-4 is a valid CAS Registry Number.

655253-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidin-7-amine

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:655253-60-4 SDS

655253-60-4Downstream Products

655253-60-4Relevant academic research and scientific papers

Novel thienopyrimidine and thiazolopyrimidine kinase inhibitors with activity against Tie-2 in vitro and in vivo

Luke, Richard W.A.,Ballard, Peter,Buttar, David,Campbell, Leonie,Curwen, Jon,Emery, Steve C.,Griffen, Alison M.,Hassall, Lorraine,Hayter, Barry R.,Jones, Cliff D.,McCoull, William,Mellor, Martine,Swain, Mike L.,Tucker, Julie A.

scheme or table, p. 6670 - 6674 (2010/06/12)

The SAR and improvement in potency against Tie2 of novel thienopyrimidine and thiazolopyrimidine kinase inhibitors are reported. The crystal structure of one of these compounds bound to the Tie-2 kinase domain is consistent with the SAR. These compounds h

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