| Identification | Back 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 Properties | Back 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) | [Appearance]
Light yellow to yellow Solid | [InChI]
InChI=1S/C5H3BrN2O3/c6-4-2-1-3(9)5(7-4)8(10)11/h1-2,9H | [InChIKey]
GSGNTVQLHGOEMB-UHFFFAOYSA-N | [SMILES]
C1([N+]([O-])=O)=NC(Br)=CC=C1O |
| Hazard Information | Back 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. | [References]
[1] Patent: WO2006/81178, 2006, A2. Location in patent: Page/Page column 22
[2] Patent: WO2006/81179, 2006, A1. Location in patent: Page/Page column 23
[3] Patent: WO2006/81264, 2006, A1. Location in patent: Page/Page column 24-25
[4] Patent: WO2006/81289, 2006, A2. Location in patent: Page/Page column 22
[5] Patent: WO2006/81182, 2006, A2. Location in patent: Page/Page column 22-23 |
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