ChemicalBook--->CAS DataBase List--->443956-08-9

443956-08-9

443956-08-9 Structure

443956-08-9 Structure
IdentificationBack Directory
[Name]

6-Bromo-2-nitro-pyridin-3-ol
[CAS]

443956-08-9
[Synonyms]

2-broMo-6-nitropyridin-3-ol
6-Bromo-2-nitro-3-pyridinol
6-Bromo-2-nitro-pyridin-3-ol
3-Pyridinol, 6-bromo-2-nitro-
6-Bromo-2-nitro-pyridine-3-ol
6-Bromo-3-hydroxy-2-nitropyridine
2-Bromo-5-hydroxy-6-nitropyridine
2-nitro-3-hydroxy-6-broMopyridine
6-Bromo-3-hydroxy-2-nitropyridine 97%
2- bromine -5- hydroxyl -6- nitropyridine
6-Bromo-2-nitro-pyridin-3-ol ISO 9001:2015 REACH
[Molecular Formula]

C5H3BrN2O3
[MDL Number]

MFCD09261204
[MOL File]

443956-08-9.mol
[Molecular Weight]

218.99
Chemical PropertiesBack Directory
[Boiling point ]

413.0±40.0 °C(Predicted)
[density ]

2.006±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

-1.31±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H332-H315-H302-H319-H312-H335
[Precautionary statements ]

P280-P302+P352-P312-P322-P363-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Uses]

6-?Bromo-?2-?nitropyridin-?3-?ol acts as a reagent for the synthesis of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad spectrum antibacterial agents. Also, functions as a reagent for the preparation of α-styrylpyridines via palladium-catalyzed coupling of N-tosylhydrazones with halopyridines, and their antitumor activity.
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