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5-bromo-1H-pyrazoio[3,4-b]pyridine

5-Bromo-1H-pyrazolo[3,4-b]pyridine

CAS: 875781-17-2

Molecular Formula: C6H4BrN3

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  5. 5-bromo-1H-pyrazoio[3,4-b]pyridine

5-bromo-1H-pyrazoio[3,4-b]pyridine - Names and Identifiers

Name 5-Bromo-1H-pyrazolo[3,4-b]pyridine
Synonyms EOS-61661
4-b]pyridine
5-broMo-1H-pyrazolo[3
7-Aza-5-bromo-1H-indole
5-Bromopyrazolo[3,4-b]pyridine
5-Bromo-1H-Pyrazo[3,4-B]Pyridine
5-BROMO-1H-PYRAZO[3,4-B]PYRIDINE
5-Bromo-1H-pyrazolo[3,4-b]pyridine
5-bromo-1H-pyrazoio[3,4-b]pyridine
5-methyl-1H-pyrazolo[3,4-b]pyridine
1H-Pyrazolo[3,4-b]pyridine, 5-bromo-
1H-Pyrazolo[3,4-b]pyridine, 5-broMo-
2H-pyrazolo[3,4-b]pyridine, 5-methyl-
CAS 875781-17-2
EINECS 807-974-3
InChI InChI=1/C7H7N3/c1-5-2-6-4-9-10-7(6)8-3-5/h2-4H,1H3,(H,8,9,10)
InChIKey BASYLPMLKGQZOG-UHFFFAOYSA-N

5-bromo-1H-pyrazoio[3,4-b]pyridine - Physico-chemical Properties

Molecular FormulaC6H4BrN3
Molar Mass198.02
Density1.894±0.06 g/cm3(Predicted)
Melting Point198.0 to 202.0 °C
Boling Point329.0±22.0 °C(Predicted)
Flash Point147.6°C
Vapor Presure0.00148mmHg at 25°C
AppearanceYellow crystal
pKa8.66±0.40(Predicted)
Storage ConditionInert atmosphere,Room Temperature
Refractive Index1.68
MDLMFCD05663982

5-bromo-1H-pyrazoio[3,4-b]pyridine - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk Codes22 - Harmful if swallowed
Safety Description24/25 - Avoid contact with skin and eyes.
WGK Germany3
HS Code29333990
Hazard ClassIRRITANT

5-bromo-1H-pyrazoio[3,4-b]pyridine - Reference Information

use 5-bromo-1H-pyrazolo [3,4-B] pyridine Chinese alias 5-bromopyrazolo [3,4-b] pyridine, pyrazolo [3,4-B] pyridine compound is a very important kind of thick heterocyclic ring, due to its specific physiological activity and structural similarity with indole, azafindole, etc., it has aroused widespread interest and is a very important type of dense heterocyclic compound. They have good curative effects in the prevention and treatment of gram-negative and positive bacteria, tumors and cancers, asthma, neurological diseases, osteoporosis and Alzheimer's disease, and have a wide range of applications in the fields of pharmaceuticals, pesticides and dyes.
Preparation When synthesizing pyrazolopyridine compounds with pyridine ring as the parent ring, hydrazine or substituted hydrazine is generally used to close the ring. If 3, 6-dichloro-2-pyridine formaldehyde reacts with hydrazine to undergo bromination reaction, 5-bromo-1H-pyrazolo [3,4-B] pyridine can be prepared. In addition, 5-bromo-1H-pyrazolo [3,4-b] pyridine can be synthesized from 2-fluoro -5-bromopyridine -3-formaldehyde in a yield of about 46%; or 5-bromo-1H-pyrazolo [3,4-b] pyridine can be synthesized from 3-aminopyrazole and 2-bromomalondialdehyde in a yield of about 11%; in this paper, 5-bromo-2-hydrazinylpyridine hydrochloride is used as the starting material to prepare 5-bromo-1H-pyrazolo [3,4-B] pyridine by intramolecular ring-forming reaction. The preparation reaction formula is as follows. Fig. 1 5-bromo-1H-pyrazolo [3,4-B] pyridine preparation reaction formula
Last Update:2024-04-09 20:49:11
5-bromo-1H-pyrazoio[3,4-b]pyridine
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View History
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