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76006-09-2

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76006-09-2 Usage

General Description

1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one, also known as RH-5849, is a chemical compound with the molecular formula C7H6N2O. It is a heterocyclic compound with a pyridine ring fused to a pyrazole ring, and a ketone group at position 7. 1,6-DIHYDRO-7H-PYRAZOLO[3,4-C]PYRIDIN-7-ONE has been studied for its potential pharmaceutical properties, particularly in the field of neuroscience and neuropharmacology. It has been investigated for its potential as a modulator of the central nervous system, particularly in relation to its ability to inhibit the enzyme cGMP-specific phosphodiesterase. Further research is ongoing to explore its potential applications in the treatment of neurological disorders and other medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 76006-09-2 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 76006-09:
(7*7)+(6*6)+(5*0)+(4*0)+(3*6)+(2*0)+(1*9)=112
112 % 10 = 2
So 76006-09-2 is a valid CAS Registry Number.

76006-09-2SDS

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 1H-pyrazolo<3,4-c>pyridin-7(6H)-one

1.2 Other means of identification

Product number -
Other names 2,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one

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:76006-09-2 SDS

76006-09-2Relevant 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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