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2-Chloro-3-methyl-5-bromopyridine

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2-Chloro-3-methyl-5-bromopyridine Basic information

Product Name:
2-Chloro-3-methyl-5-bromopyridine
Synonyms:
  • 5-BROMO-2-CHLORO-3-PICOLINE
  • 5-BROMO-2-CHLORO-3-METHYLPYRIDINE
  • 2-CHLORO-3-METHYL-5-BROMO PYRIDINE
  • 2-CHLORO-5-BROMO-3-PICOLINE
  • 2-Chloro-5-bromo-3-methylpyridine
  • 5-Bromo-2-chloro-3-methylpyridine ,98%
  • 5-Bromo-2-chloro-3-picoline,98%
  • 5-BROMO-2-CHLORO-3-PICOLINE (5-BROMO-2-CHLORO-3-METHYLPYRIDINE)
CAS:
29241-60-9
MF:
C6H5BrClN
MW:
206.47
Product Categories:
  • Pyridine
  • Pyridine series
  • Pyridines
  • Boronic Acid
  • Heterocycle-Pyridine series
  • compounds of pyridine
Mol File:
29241-60-9.mol
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2-Chloro-3-methyl-5-bromopyridine Chemical Properties

Melting point:
40-44 °C
Boiling point:
78°C/3mmHg(lit.)
Density 
1.6567 (rough estimate)
refractive index 
1.5400 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1?+-.0.10(Predicted)
form 
Solid
color 
White to Almost white
CAS DataBase Reference
29241-60-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39
HazardClass 
IRRITANT
HS Code 
29333990

MSDS

  • Language:English Provider:ACROS
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2-Chloro-3-methyl-5-bromopyridine Usage And Synthesis

Chemical Properties

white to light beige crystalline powder

Synthesis

89488-30-2

29241-60-9

Example 11B Synthesis of 5-bromo-2-chloro-3-methylpyridine: The product of Example 11A, 5-bromo-3-methylpyridin-2-one (4.1 g, 22.18 mmol), was dissolved in DMF (40 mL) and phosphoryl chloride (10 g, 65.4 mmol) was added drop-wise at 0 °C. The reaction mixture was heated at 120 °C for 2 hours. Upon completion of the reaction, the mixture was cooled to room temperature and carefully poured into an ice/water mixture. The mixture was adjusted to alkaline with NH4OH, the precipitate was collected by filtration and the filter cake was washed with ice water. The resulting solid was dissolved in dichloromethane (100 mL), the organic layer was washed with brine and dried with anhydrous MgSO4. The dried solution was filtered through a silica pad and the filtrate was concentrated to give 2-chloro-3-methyl-5-bromopyridine as a white solid (3.48 g, 78% yield). The product was characterized by 1H NMR (CDCl3, 300MHz): δ 2.39 (s, 3H), 7.70 (m, 1H), 8.31 (d, J = 3Hz, 1H).

References

[1] Patent: US2002/19388, 2002, A1
[2] Patent: EP1428824, 2004, A1. Location in patent: Page 49

2-Chloro-3-methyl-5-bromopyridine Preparation Products And Raw materials

Raw materials

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