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3-BROMO-2-METHYLBENZONITRILE

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3-BROMO-2-METHYLBENZONITRILE Basic information

Product Name:
3-BROMO-2-METHYLBENZONITRILE
Synonyms:
  • 3-Bromo-2-methylbenzonitrile 98%
  • 3-Bromo-2-methylbenzonitrile98%
  • 3-BROMO-2-METHYLBENZONITRILE
  • Benzonitrile, 3-bromo-2-methyl-
CAS:
52780-15-1
MF:
C8H6BrN
MW:
196.04
Mol File:
52780-15-1.mol
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3-BROMO-2-METHYLBENZONITRILE Chemical Properties

Melting point:
44-45 °C
Boiling point:
247.5±20.0 °C(Predicted)
Density 
1.51±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
Appearance
White to light yellow Solid
InChI
InChI=1S/C8H6BrN/c1-6-7(5-10)3-2-4-8(6)9/h2-4H,1H3
InChIKey
VJMRAGHVKBZNAF-UHFFFAOYSA-N
SMILES
C(#N)C1=CC=CC(Br)=C1C
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
RIDADR 
2811
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2926907090
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3-BROMO-2-METHYLBENZONITRILE Usage And Synthesis

Uses

3-Bromo-2-methylbenzonitrile is an organic compound commonly used as an intermediate in organic synthesis, especially in pharmaceutical and pesticide chemistry.

Synthesis

919363-09-0

407-25-0

52780-15-1

A solution of 3-bromo-2-methylbenzamide (500 mg, 2.340 mmol) and pyridine (0.60 mL, 7.42 mmol) in dichloromethane (10 mL) was cooled to 0 °C and then trifluoroacetic anhydride (1.0 mL, 7.08 mmol) was slowly added. The reaction mixture was gradually warmed to room temperature and stirred continuously for 15 hours. Upon completion of the reaction, the mixture was partitioned between ethyl acetate (100 mL) and 1M HCl solution (25 mL). The organic phase was washed sequentially with saturated NaHCO3 solution (25 mL) and brine (25 mL), dried over Na2SO4, filtered and concentrated to give 423 mg (92%) of 3-bromo-2-methylbenzonitrile as a light yellow oil, which could be used for the next reaction without further purification.

References

[1] Patent: WO2007/76247, 2007, A1. Location in patent: Page/Page column 46-48

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