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100859-35-6

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100859-35-6 Usage

Purine derivative

Contains a pyrimidine ring fused to an imidazole ring
Chlorinated and methylated derivative of purine
Used in the synthesis of pharmaceuticals and organic compounds
Alters chemical properties and biological activities
Important intermediate in the synthesis of nucleoside analogs and pharmaceuticals like antiviral and anticancer drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 100859-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,5 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100859-35:
(8*1)+(7*0)+(6*0)+(5*8)+(4*5)+(3*9)+(2*3)+(1*5)=106
106 % 10 = 6
So 100859-35-6 is a valid CAS Registry Number.

100859-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-methyl-7H-purine

1.2 Other means of identification

Product number -
Other names 1H-Purine,6-chloro-2-methyl

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:100859-35-6 SDS

100859-35-6Relevant articles and documents

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Goldman et al.

, p. 599 (1956)

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TRANSGLUTAMINASE 2 (TG2) INHIBITORS

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, (2020/03/02)

Described herein are compounds and pharmaceutical compositions containing such compounds which inhibit transglutaminase 2 (TG2). Also described herein are methods for using such TG2 inhibitors, alone or in combination with other compounds, for treating diseases or conditions that would benefit from TG2 inhibition.

COMPOSITIONS AND METHODS USING THE SAME FOR TREATMENT OF NEURODEGENERATIVE AND MITOCHONDRIAL DISEASE

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Page/Page column 139; 140, (2015/09/22)

The present disclosure is directed, in part, to compounds, or pharmaceutically acceptable salts thereof, for the treatment and/or prevention of neurodegenerative disease and/or mitchonodrial disease including Parkinson's disease and Leigh's disease.

Bioisosteric transformations and permutations in the triazolopyrimidine scaffold to identify the minimum pharmacophore required for inhibitory activity against plasmodium falciparum dihydroorotate dehydrogenase

Marwaha, Alka,White, John,El-mazouni, Farah,Creason, Sharon A,Kokkonda, Sreekanth,Buckner, Frederick S.,Charman, Susan A.,Phillips, Margaret A.,Rathod, Pradipsinh K.

, p. 7425 - 7436 (2012/11/07)

Plasmodium falciparum causes approximately 1 million deaths annually. However, increasing resistance imposes a continuous threat to existing drug therapies. We previously reported a number of potent and selective triazolopyrimidine-based inhibitors of P.

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