ChemicalBook--->CAS DataBase List--->15862-37-0

15862-37-0

15862-37-0 Structure

15862-37-0 Structure
IdentificationMore
[Name]

2,5-Dibromo-3-nitropyridine
[CAS]

15862-37-0
[Synonyms]

2,5-Dibromo-3-nitropyridine
[EINECS(EC#)]

808-084-8
[Molecular Formula]

C5H2Br2N2O2
[MDL Number]

MFCD09266223
[Molecular Weight]

281.89
[MOL File]

15862-37-0.mol
Chemical PropertiesBack Directory
[Melting point ]

92.0 to 96.0 °C
[Boiling point ]

272.7±35.0 °C(Predicted)
[density ]

2?+-.0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[solubility ]

soluble in Methanol
[form ]

Solid
[pka]

-5.60±0.20(Predicted)
[color ]

Yellow
[InChIKey]

OQKWPJCAKRVADO-UHFFFAOYSA-N
[CAS DataBase Reference]

15862-37-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sulfuric acid-->Nitric acid-->Government regulation-->Sodium nitrite-->Hydrogen bromide-->Sodium thiosulfate-->2-Aminopyridine
[Preparation Products]

5-Bromo-3-nitropyridine-2-carbonitrile-->5-BROMO-3-FLUORO-PYRIDINE-2-CARBONITRILE-->2,5-Dimethyl-3-nitropyridine
Hazard InformationBack Directory
[Uses]

2,5-Dibromo-3-nitropyridine is used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
[Preparation]

synthesis of 2,5-Dibromo-3-nitropyridine: To a suspension 5-bromo-3-nitro-pyridin-2-ol (20 g, 91.32 mmol) in toluene (100 ml) was added DMF (0.7 ml, 9.13 mmol) and the mixture was heated to 90??C. (the reaction mixture was protected from light). A solution of POBr3 (31. 41 g, 109.51 mmol) in toluene (40 ml) was added dropwise at 90??C. and the reaction mixture was stirred at that temperature for 16 h. The mixture was allowed to cool to room temperature and toluene (50 ml) and water (50 ml) were added. The organic layer was separated, washed successively with aqueous 1N NaOH (60 ml), water (60 ml) and brine (30 ml), dried with Na2SO4 and evaporated obtain 2,5-Dibromo-3-nitropyridine. Yellow solid, yield 25.2 g, 97%.
15862-37-0 synthesis
Spectrum DetailBack Directory
[Spectrum Detail]

2,5-Dibromo-3-nitropyridine(15862-37-0)1HNMR
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