| Identification | Back Directory | [Name]
3,5-Dibromo-2-methylpyridine | [CAS]
38749-87-0 | [Synonyms]
3,5-Dibromo-2-methyl
3,5-Dibromo-2-picoline
3,5-Bibromo-2-methylpyridine
Pyridine, 3,5-dibromo-2-methyl-
3,5-Dibromo-2-methylpyridine 98+%
3,5-Dibromo-2-methylpyridine ISO 9001：2015 REACH | [Molecular Formula]
C6H5Br2N | [MDL Number]
MFCD00234159 | [MOL File]
38749-87-0.mol | [Molecular Weight]
250.92 |
| Chemical Properties | Back Directory | [Boiling point ]
227.9±35.0 °C(Predicted) | [density ]
1.911±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
solid | [pka]
1.24±0.20(Predicted) | [color ]
White to off white |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 2-methyl-3,5-dibromo-6-methylpyridine from 2-amino-3,5-dibromo-6-methylpyridine: tert-butyl nitrite (1.5 mL, 12.6 mmol) was added to a solution of 2-amino-3,5-dibromo-6-methylpyridine (2.0 g, 7.5 mmol) in tetrahydrofuran (THF, 75 mL). The reaction mixture was heated to reflux and kept for 2 hours. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography (SiO2, dichloromethane as eluent) to afford the target product 2-methyl-3,5-dibromopyridine (0.8 g, 42% yield). High performance liquid chromatography (HPLC) analysis showed a retention time (Rt) of 2.77 min. | [References]
[1] Patent: US2005/192310, 2005, A1. Location in patent: Page/Page column 35 |
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| Company Name: |
Energy Chemical
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| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
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