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21410-06-0

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  • SAGECHEM/3-Benzyl-7-chloro-3H-[1,2,3]triazolo[4,5-d]pyrimidine/SAGECHEM/Manufacturer in China

    Cas No: 21410-06-0

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21410-06-0 Usage

General Description

3-Benzyl-7-chloro-3H-[1,2,3]triazolo[4,5-d]pyrimidine is a chemical compound that belongs to the triazolopyrimidine family. It is characterized by a benzene ring attached to the triazolo[4,5-d]pyrimidine core structure, along with a chlorine substituent at the 7th position. 3-BENZYL-7-CHLORO-3H-[1,2,3]TRIAZOLO[4,5-D]PYRIMIDINE is of interest in medicinal and pharmaceutical research due to its potential biological activities, including antiviral and anticancer properties. The unique structure of 3-benzyl-7-chloro-3H-[1,2,3]triazolo[4,5-d]pyrimidine makes it a valuable candidate for drug development and further study in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 21410-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21410-06:
(7*2)+(6*1)+(5*4)+(4*1)+(3*0)+(2*0)+(1*6)=50
50 % 10 = 0
So 21410-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H8ClN5/c12-10-9-11(14-7-13-10)17(16-15-9)6-8-4-2-1-3-5-8/h1-5,7H,6H2

21410-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-7-chlorotriazolo[4,5-d]pyrimidine

1.2 Other means of identification

Product number -
Other names 3-benzyl-7-chloro-1,2,3-triazolo[4,5-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:21410-06-0 SDS

21410-06-0Relevant articles and documents

Cytoprotective activities of kinetin purine isosteres

Maková, Barbara,Mik, Václav,Li?ková, Barbora,Gonzalez, Gabriel,Vítek, Dominik,Medvedíková, Martina,Monfort, Beata,Ru?ilová, Veronika,Kadlecová, Alena,Khirsariya, Prashant,Gándara Barreiro, Zoila,Havlí?ek, Libor,Zatloukal, Marek,Soural, Miroslav,Paruch, Kamil,D'Autréaux, Benoit,Hajdúch, Marián,Strnad, Miroslav,Voller, Ji?í

, (2021/01/28)

Kinetin (N6-furfuryladenine), a plant growth substance of the cytokinin family, has been shown to modulate aging and various age-related conditions in animal models. Here we report the synthesis of kinetin isosteres with the purine ring replace

Compounds containing a N-heteroaryl moiety linked to fused ring moieties for the inhibition of NAD(P)H oxidases and platelet activation

-

Page/Page column 88, (2008/06/13)

The invention relates to compounds containing a N-heteroaryl moiety, which is linked via oxygen, sulfur or nitrogen, or via a methylene bridge and oxygen, sulfur or nitrogen to a fused ring moiety, in particular to the 1,2,3-triazolo[4,5-d]pyrimidine-7-yl radical. The invention also relates to a process for the preparation of said compounds and the use thereof in drugs for the treatment of NAD(P)H oxidases-related diseases and disorders and inhibition of platelet activation.

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