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3-Bromo-6-methoxy-2-picoline

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3-Bromo-6-methoxy-2-picoline Basic information

Product Name:
3-Bromo-6-methoxy-2-picoline
Synonyms:
  • 3-BROMO-6-METHOXY-2-METHYLPYRIDINE
  • 3-BROMO-6-METHOXY-2-PICOLINE
  • 2-METHOXY-5-BROMO-6-PICOLINE
  • 2-METHYL-3-BROMO-6-METHOXY PYRIDINE
  • 5-Bromo-2-Methoxy-6-Methylpyridine
  • Pyridine, 3-broMo-6-Methoxy-2-Methyl-
  • 5-Bromo-2-methoxy-6-picoline
  • 5-Bromo-2-methoxy-6-methylpyridine, 3-Bromo-6-methoxy-2-picoline
CAS:
126717-59-7
MF:
C7H8BrNO
MW:
202.05
Product Categories:
  • Heterocycle-Pyridine series
  • Pyridine Series
  • C7 to C18
  • Building Blocks
  • C7 to C8
  • Chemical Synthesis
  • Pyridine
  • Pyridines
  • Boronic Acid
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • New Products for Chemical Synthesis
Mol File:
126717-59-7.mol
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3-Bromo-6-methoxy-2-picoline Chemical Properties

Boiling point:
86°C/10mmHg(lit.)
Density 
1.468g/mLat 25℃
refractive index 
n20/D 1.548
Flash point:
106°C
storage temp. 
2-8°C
pka
1.76±0.10(Predicted)
form 
Liquid
color 
Colorless
CAS DataBase Reference
126717-59-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
41-22
Safety Statements 
26-39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933399990
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3-Bromo-6-methoxy-2-picoline Usage And Synthesis

Synthesis

A mixture of 5-bromo-6-methyl-1H-pyridin- 2-one (5.5 g, 29 mmol), silver carbonate (10.89 g, 39 mmol), iodomethane (13.6 mL, 217 mmol) and chloroform (115 mL) is stirred overnight in the dark at room temperature. Triethylamine (10 mL) is added, and stirring is continued for 1.5 hr. The reaction mixture is filtered through a pad of Hi-Flo, and the filtrate is washed with water (100 mL), dried, filtered and concentrated. The residue is purified by filtration through a pad of silica gel washing with cyclohexane-20percent ethyl acetate. The solvent is concentrated to afford 3-Bromo-6-methoxy-2-picoline (3.7 g, 63percent yield) as an oil.

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