76006-14-9

Basic information

• Product Name: 3-Chloro-1H-pyrazolo[3,4-c]pyridine
• Synonyms: 3-Chloro-1H-pyrazolo[3,4-c]pyridine;1H-Pyrazolo[3,4-c]pyridine, 3-chloro-
• CAS NO: 76006-14-9
• Molecular Formula: C6H4ClN3
• Molecular Weight: 153.572
• Mol File: 76006-14-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Chloro-1H-pyrazolo[3,4-c]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloro-1H-pyrazolo[3,4-c]pyridine(76006-14-9)
• EPA Substance Registry System: 3-Chloro-1H-pyrazolo[3,4-c]pyridine(76006-14-9)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 45
• RIDADR: UN 2811 6.1 / PGIII
• Hazardous Substances Data: 76006-14-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Synthesis:
3-Chloro-1H-pyrazolo[3,4-c]pyridine is used as an intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs with diverse biological activities.
Used in Agricultural Chemicals:
In the agricultural sector, 3-Chloro-1H-pyrazolo[3,4-c]pyridine is used as a precursor in the production of agricultural chemicals, potentially enhancing crop protection and yield.
Used in Organic Chemistry Research:
3-Chloro-1H-pyrazolo[3,4-c]pyridine serves as a valuable building block in organic chemistry research, facilitating the construction of complex organic molecules for further exploration of their properties and applications.
Used in Medicinal Chemistry and Drug Development:
In the fields of medicinal chemistry and drug development, 3-Chloro-1H-pyrazolo[3,4-c]pyridine is utilized for its potential to be incorporated into novel drug candidates, contributing to the advancement of therapeutic agents with improved efficacy and selectivity.

Upstream product

• 271-47-6 1H-pyrazolo[3,4-c]pyridine 

Relevant articles and documents

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

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

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.