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76006-06-9

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76006-06-9 Usage

General Description

5-Methyl-1H-pyrazolo[3,4-c]pyridine is a chemical compound with the molecular formula C8H7N3. It is a heterocyclic compound that consists of a pyridine ring fused to a pyrazole ring. 5-METHYL-1H-PYRAZOLO[3,4-C]PYRIDINE is used in the pharmaceutical industry as a building block for the synthesis of various drug molecules, particularly in the development of new pharmaceuticals. It has also been studied for its potential biological and pharmacological activities, such as its role as a potential antiviral agent. Additionally, it has been investigated for its potential use in the treatment of various diseases and disorders. The compound has also been studied for its potential use in organic synthesis for the creation of new chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 76006-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76006-06:
(7*7)+(6*6)+(5*0)+(4*0)+(3*6)+(2*0)+(1*6)=109
109 % 10 = 9
So 76006-06-9 is a valid CAS Registry Number.

76006-06-9 Well-known Company Product Price

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  • Aldrich

  • (BLN00020)  5-Methyl-1H-pyrazolo[3,4-c]pyridine  AldrichCPR

  • 76006-06-9

  • BLN00020-1G

  • 12,249.90CNY

  • Detail

76006-06-9SDS

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 5-methyl-1H-pyrazolo[3,4-c]pyridine

1.2 Other means of identification

Product number -
Other names 1H-PYRAZOLO[3,4-C]PYRIDINE,5-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:76006-06-9 SDS

76006-06-9Relevant articles and documents

Pyrazolopyridines. Part 5. Preparation and Reactions of Pyrazolopyridines

Chapman, David,Hurst, Jim

, p. 2398 - 2404 (2007/10/02)

A series of pyrazolopyridines has been prepared by nitrosation of 3-acetamido-4-methylpyridines and subsequent rearrangement and cyclisation of the N-acetyl-N-nitroso-compounds produced.The reactions of the pyrazolopyridines have been investigated. 1- and 2-Acetyl and 1- and 2-benzyl compounds were obtained and their structures elucidated spectroscopically.The ring system readily undergoes electrophilic substitution in the 3-position. 7-Chloropyrazolopyridine has been shown to be more susceptible to nucleophilic substitution than the isomeric 5-chloro-compound.

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