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5334-32-7

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5334-32-7 Usage

Class

pyrazolopyrimidine derivatives

Structure

Pyrimidine ring fused with a pyrazole ring, with two sulfur atoms attached to carbon atoms at positions 4 and 6

Pharmaceutical applications

Potential use in the treatment of cancer and inflammation due to the ability to inhibit certain enzymes and receptors in the body

Fluorescent probe potential

Has been investigated for its potential use in biological and environmental monitoring

Check Digit Verification of cas no

The CAS Registry Mumber 5334-32-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5334-32:
(6*5)+(5*3)+(4*3)+(3*4)+(2*3)+(1*2)=77
77 % 10 = 7
So 5334-32-7 is a valid CAS Registry Number.

5334-32-7SDS

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 1,2-dihydropyrazolo[3,4-d]pyrimidine-4,6-dithione

1.2 Other means of identification

Product number -
Other names 1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione

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:5334-32-7 SDS

5334-32-7Relevant articles and documents

Synthesis and biological evaluation of some acyclic 4,6-disubstituted 1H-pyrazolo[3,4-d]pyrimidine nucleosides

Moukha-Chafiq,Taha,Mouma,Lazrek,Vasseur,De Clercq

, p. 967 - 972 (2007/10/03)

The chemical synthesis and biological evaluation of some acyclic α-[6-(1′-carbamoylalkylthio)-1H-pyrazolo[3,4-d]pyrimidin-4-yl] thioalkylamide nucleosides are described.

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