Basic information Safety Supplier Related

4-BROMO-2-METHYLTHIAZOLE

Basic information Safety Supplier Related

4-BROMO-2-METHYLTHIAZOLE Basic information

Product Name:
4-BROMO-2-METHYLTHIAZOLE
Synonyms:
  • 4-BROMO-2-METHYLTHIAZOLE
  • 4-Bromo-2-methyl-1,3-thiazole
  • 4-Bromo-2-(methyl-d3)-thiazole
  • Thiazole, 4-bromo-2-methyl-
  • 4-Bromo-2-methylthiazole 98%
CAS:
298694-30-1
MF:
C4H4BrNS
MW:
178.05
Mol File:
298694-30-1.mol
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4-BROMO-2-METHYLTHIAZOLE Chemical Properties

Boiling point:
199.2±13.0 °C(Predicted)
Density 
1.702±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
0.66±0.10(Predicted)
form 
liquid
color 
Colourless
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Safety Information

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-39
Hazard Note 
Irritant
HS Code 
2934100090
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4-BROMO-2-METHYLTHIAZOLE Usage And Synthesis

Synthesis

616-42-2

298694-30-1

General procedure for the synthesis of 2-methyl-4-bromothiazole from dimethyl sulfite: 2,4-dibromothiazole (2.4 g, 9.8 mmol) was dissolved in anhydrous THF (50 mL), and the resulting solution was stirred at -78 °C under argon protection. Slowly n-butyllithium (4.2 mL, 6 mmol, 2.5 M hexane solution) was added and stirring was continued for 1 hour. Subsequently, a solution of dimethyl sulfate (2.7 mL) in THF (5 mL) was added dropwise. The reaction mixture was stirred at -78 °C for 4 h before slowly warming to room temperature and continuing to stir overnight. Upon completion of the reaction, the reaction mixture was diluted with saturated aqueous sodium bicarbonate solution (50 mL). The aqueous layer was extracted with ether, the organic phases were combined, washed with brine, dried over magnesium sulfate and concentrated by rotary evaporation. Finally, purification by silica gel column chromatography afforded 2-methyl-4-bromothiazole as a yellow oil (0.956 g, 55% yield).

References

[1] Patent: WO2007/14922, 2007, A1. Location in patent: Page/Page column 121-122

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