| Identification | Back Directory | [Name]
(5-nitropyridin-2-yl)hydrazine | [CAS]
6343-98-2 | [Synonyms]
2-Hydrazinyl-5-nitropyridine
(5-nitro-2-pyridyl)hydrazine
(5-nitropyridin-2-yl)hydrazine
Pyridine, 2-hydrazinyl-5-nitro-
6-hydrazino-N-hydroxy-3-pyridinamine oxide
6-hydrazino-N-hydroxy-pyridin-3-amine oxide
6-hydrazinyl-N-hydroxypyridin-3-amine oxide
6-hydrazinyl-N-hydroxy-pyridin-3-amine oxide
N-(6-hydrazino-3-pyridyl)-N-oxidohydroxylamine
N-(6-hydrazino-3-pyridyl)-N-oxido-hydroxylamine
N-(6-hydrazinylpyridin-3-yl)-N-oxidohydroxylamine
N-(6-hydrazinylpyridin-3-yl)-N-oxido-hydroxylamine
(5-nitropyridin-2-yl)hydrazine ISO 9001：2015 REACH | [Molecular Formula]
C5H6N4O2 | [MDL Number]
MFCD00118332 | [MOL File]
6343-98-2.mol | [Molecular Weight]
154.13 |
| Chemical Properties | Back Directory | [Melting point ]
205-206 °C (decomp) | [Boiling point ]
266.3±43.0 °C(Predicted) | [density ]
1.60±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | [form ]
solid | [pka]
4.13±0.70(Predicted) | [color ]
Green |
| Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 2-hydrazino-5-nitropyridine from 2-chloro-5-nitropyridine was as follows: 47.6 g (0.3 mol) of 2-chloro-5-nitropyridine was suspended in a solvent mixture of 400 ml of methanol and 60 ml of water, prepared as a slurry and cooled to 10 °C. The above slurry was slowly added to 86 g of 95% hydrazine solution cooled to below 30°C under stirring and the addition time was controlled to be more than 10 minutes. During the reaction, the solid first dissolved and subsequently precipitated a yellow-green precipitate. The reaction mixture was heated to reflux and stirred continuously for 30 minutes. Upon completion of the reaction, the light green solid product was collected by filtration and washed with cold methanol. The resulting solid was resuspended in 200 mL of cold water, washed and dried under vacuum to give 40.1 g of 2-hydrazino-5-nitropyridine in 87% yield. | [References]
[1] Journal of Medicinal Chemistry, 1997, vol. 40, # 26, p. 4420 - 4425
[2] Patent: GB255811,
[3] Patent: US1733695,
[4] Chem.Abstr., 1927, vol. 21, p. 594
[5] Patent: GB247188, |
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