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637338-77-3

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637338-77-3 Usage

Chemical structure

A derivative of pyrazolopyrimidine with a chlorine atom attached

Usage

As a building block for the synthesis of various organic compounds in the pharmaceutical industry

Potential applications

In the treatment of various diseases and disorders, including cancer and inflammatory conditions

Ongoing research and development

Yes

Other possible uses

As an agricultural chemical or in other industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 637338-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,3,3 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 637338-77:
(8*6)+(7*3)+(6*7)+(5*3)+(4*3)+(3*8)+(2*7)+(1*7)=183
183 % 10 = 3
So 637338-77-3 is a valid CAS Registry Number.

637338-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-chloro-

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:637338-77-3 SDS

637338-77-3Downstream Products

637338-77-3Relevant articles and documents

Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: Synthesis, deamination and tautomerism

Seela, Frank,Xu, Kuiying

, p. 3034 - 3045 (2008/04/01)

The syntheses and properties of 8-aza-7-deazapurine (pyrazolo[3,4-d] pyrimidine) ribonucleosides related to 2-aminoadenosine and isoguanosine are described. Glycosylation of 8-aza-7-deazapurine-2,6-diamine 5 with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-d-ribofur

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