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ChemicalBook--->CAS DataBase List--->26944-71-8

26944-71-8

26944-71-8 Structure

26944-71-8 Structure
IdentificationBack Directory
[Name]

2-BROMO-6-HYDRAZINYLPYRIDINE
[CAS]

26944-71-8
[Synonyms]

2-Bromo-6-hydrazinopydine
2-Bromo-6-hydrazinopyridine
2-Diazanyl-6-Bromo Pyridine
2-hydrazine-6-bromopyridine
2-BROMO-6-HYDRAZINYLPYRIDINE
(6-bromo-2-pyridyl)hydrazine
(6-Bromopyridin-2-yl)hydrazine
Pyridine, 2-bromo-6-hydrazinyl-
2-Bromo-6-hydrazinopyridine,98%
1-(6-bromopyridin-2-yl)hydrazine
2-Bromo-6-hydrazinopyridine 97+%
2-(6-bromopyridin-2-yl)hydrazine
2-bromo-6-hydrazinopyridine hydrochloride
2-bromo-6-hydrazinopyridine(SALTDATA: HCl)
(E)-6-bromo-2-hydrazono-1,2-dihydropyridine
2-BROMO-6-HYDRAZINYLPYRIDINE ISO 9001:2015 REACH
[Molecular Formula]

C5H6BrN3
[MDL Number]

MFCD09743754
[MOL File]

26944-71-8.mol
[Molecular Weight]

188.02
Chemical PropertiesBack Directory
[Melting point ]

117-118℃
[Boiling point ]

265.9±50.0 °C(Predicted)
[density ]

1.82±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[solubility ]

soluble in Methanol
[form ]

Solid
[pka]

9.08±0.70(Predicted)
[color ]

Pale brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS05,GHS06
[Signal word ]

Warning
[Hazard statements ]

H301-H315-H318-H335
[Precautionary statements ]

P261-P280a-P301+P310a-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[HazardClass ]

6.1
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

2-Bromo-6-hydrazinylpyridine is used as an intermediate in organic synthesis for the production and research of other compounds.
[Synthesis]

2,6-Dibromopyridine

626-05-1

2-BROMO-6-HYDRAZINYLPYRIDINE

26944-71-8

General procedure for the synthesis of 2-bromo-6-hydrazinopyridine from 2,6-dibromopyridine: commercially available 2,6-dibromopyridine (4.12 g, 16.6 mmol) was suspended in ethanol (40 mL), followed by the addition of hydrazine hydrate (10 mL, 97.6 mmol, 50-60% aqueous solution). The reaction mixture was heated and refluxed in a sand bath at 115°C for 18 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the resulting residue was purified by silica gel column chromatography with the eluent ethyl acetate/n-heptane (60/40, v/v) to afford 2-bromo-6-hydrazinopyridine as an off-white solid (3.05 g, 93% yield).1H-NMR (400 MHz, CDCl3) δ: 7.33 (t, 1H), 6.83 (d, 1H ), 6.67 (d, 1H), 6.00 (br-s, 1H), 3.00-3.33 (br-s, 2H).

[References]

[1] Patent: US2011/256064, 2011, A1. Location in patent: Page/Page column 22
[2] Patent: EP2377860, 2011, A1. Location in patent: Page/Page column 29
[3] Patent: US2011/280808, 2011, A1. Location in patent: Page/Page column 54
[4] Patent: WO2015/110263, 2015, A1. Location in patent: Page/Page column 159
[5] Patent: US2017/2005, 2017, A1. Location in patent: Paragraph 0760; 0761; 0762; 0763
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