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90213-35-7

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90213-35-7 Usage

Chemical Family

pyrazolopyrimidine
A chemical family consisting of compounds with a pyrazole ring fused to a pyrimidine ring.

Derivative

carbothioamide
A derivative of a parent compound, modified by the addition of a carbothioamide group.

Substituent

methylthio group
A chemical group (-CH3-SH) attached to the fourth position of the pyrazolopyrimidine ring, influencing the compound's properties and reactivity.

Molecular Structure

1H-Pyrazolo[3,4-d]pyrimidine-3-carbothioamide, 4-(methylthio)-
The molecular formula and structure of the compound, which includes a pyrazolo[3,4-d]pyrimidine core with a carbothioamide group and a methylthio substituent.

Biological Interaction

potential pharmaceutical and medicinal properties
The ability of the compound to interact with biological systems, making it a candidate for drug development and medicinal applications.

Disease Treatment

potential use in treating various diseases
The possibility that the compound may be effective in treating different diseases due to its unique structure and properties.

Research and Development

candidate for further study in drug discovery and medicinal chemistry
The compound's molecular structure and properties make it a promising candidate for additional research in the fields of drug discovery and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 90213-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90213-35:
(7*9)+(6*0)+(5*2)+(4*1)+(3*3)+(2*3)+(1*5)=97
97 % 10 = 7
So 90213-35-7 is a valid CAS Registry Number.

90213-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylsulfanyl-2H-pyrazolo[3,4-d]pyrimidine-3-carbothioamide

1.2 Other means of identification

Product number -
Other names 3-Thiocarbamoyl-4-methylmercaptopyrazolo<3,4-d>pyrimidine

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:90213-35-7 SDS

90213-35-7Downstream Products

90213-35-7Relevant articles and documents

SYNTHESIS OF 3-SUBSTITUTED 4-METHYLMERCAPTO- AND 4-AMINOPYRAZOLOPYRIMIDINES AND THEIR RIBOSIDES

Bulychev, Yu. N.,Korbukh, I. A.,Preobrazhenskaya, M. N.

, p. 210 - 215 (2007/10/02)

3-Cyano-4-methylmercaptopyrazolopyrimidine, fusion of which with 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose gave its per-O-acetylated 1-β-D-ribofuranoside in 61percent yield, was synthesized from 3,4-dicyano-5-aminopyrazole.O-Deacetylation of the per-O-acetylated 1-β-D-ribofuranoside was carried out by the action of 1percent HCl in methanol. New pyrazolopyrimidines were obtained by the reaction of 3-cyano-4-methylmercaptopyrazolopyrimidine and its 1-riboside, as well as 3-cyano-4-aminopyrazolopyrimidine, with a number of nucleophilic reagents.The cytotoxic activities of the compounds obtained were studied.

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