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439692-52-1

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439692-52-1 Usage

Uses

4-Chloro-6-isopropylthieno[2,3-d]pyrimidine, is a building block used in the synthesis of various compounds such as 4-((7H-Pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-pyrazole-3-carboxamide (FN-1501), as FLT3- and CDK-Kinase Inhibitor with Potentially High Efficiency against Acute Myelocytic Leukemia.

Check Digit Verification of cas no

The CAS Registry Mumber 439692-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 439692-52:
(8*4)+(7*3)+(6*9)+(5*6)+(4*9)+(3*2)+(2*5)+(1*2)=191
191 % 10 = 1
So 439692-52-1 is a valid CAS Registry Number.

439692-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-6-propan-2-ylthieno[2,3-d]pyrimidine

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:439692-52-1 SDS

439692-52-1Relevant articles and documents

INHIBITORS OF NOTUM PECTINACETYLESTERASE AND METHODS OF THEIR USE

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Page/Page column 12, (2012/03/27)

Compounds are disclosed for the treatment, management and prevention of diseases and disorders affecting the bone. Particular compounds are potent inhibitors of Notum Pectinacetylesterase, and are of the formula: wherein E, G, Y, Z, R1, R2, and R3 are defined herein.

New piperidinylamino-thieno[2,3-D] pyrimidine compounds

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, (2008/06/13)

The invention relates to 5-HT receptor antagonists. Novel piperidinylamino-thieno [2,3-d]pyrimidine compounds represented by Formula I, and synthesis and uses thereof for treating diseases mediated directly or indirectly by 5-HT receptors, are disclosed.

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