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3-Bromo-1H-pyrazolo[3,4-c]pyridine is a heterocyclic compound characterized by the presence of a pyrazolo[3,4-c]pyridine ring system with a bromine atom at the 3-position. This unique molecular structure endows it with specific chemical properties and reactivity, making it a valuable intermediate in organic synthesis and medicinal chemistry.

76006-13-8

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76006-13-8 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-1H-pyrazolo[3,4-c]pyridine is used as a key reactant for the synthesis of azaindazoles, which are potent inhibitors of bacterial DNA ligase. These inhibitors play a crucial role in the development of new antimicrobial agents, as they target essential enzymes involved in bacterial DNA replication and repair processes. By inhibiting bacterial DNA ligase, azaindazoles can effectively disrupt the growth and survival of various pathogenic bacteria, offering a promising strategy for combating antibiotic-resistant infections.

Check Digit Verification of cas no

The CAS Registry Mumber 76006-13-8 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, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76006-13:
(7*7)+(6*6)+(5*0)+(4*0)+(3*6)+(2*1)+(1*3)=108
108 % 10 = 8
So 76006-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BrN3/c7-6-4-1-2-8-3-5(4)9-10-6/h1-3H,(H,9,10)

76006-13-8 Well-known Company Product Price

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  • Aldrich

  • (BLN00004)  3-Bromo-1H-pyrazolo[3,4-c]pyridine  AldrichCPR

  • 76006-13-8

  • BLN00004-1G

  • 3,540.42CNY

  • Detail

76006-13-8SDS

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 3-Bromo-1H-pyrazolo[3,4-c]pyridine

1.2 Other means of identification

Product number -
Other names 3-bromo-2H-pyrazolo[3,4-c]pyridine

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:76006-13-8 SDS

76006-13-8Downstream Products

76006-13-8Relevant academic research and scientific papers

Heterocyclic substituted 2-methyl-benzimidazole antiviral agents

-

, (2008/06/13)

The present invention concerns antiviral compounds, their methods of preparation and their compositions, and use in the treatment of viral infections. More particularly, the invention provides heterocyclic substituted 2-methylbenzimidazole derivatives for the treatment of respiratory syncytial virus infection.

Synthesis, reactivity and 13C-NMR of 1H-pyrazolo[3,4-c]pyridine derivatives

Milhavet, Jean-Claude,Gueiffier, Alain,Bernal, Lysiane,Teulade, Jean-Claude

, p. 1661 - 1667 (2007/10/03)

The synthesis of various 1H-pyrazolo [.-c.]pyridines was reported. 3- Cyano derivatives were obtained from the corresponding nitro compounds by Sandmeyer Reaction using Na3[Cu(CN)4] at pH 1. The 13C-NMR data of this series were also described.

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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