Basic information Safety Supplier Related

(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile

Basic information Safety Supplier Related

(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile Basic information

Product Name:
(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile
Synonyms:
  • 1H-Benzimidazole-2-acetonitrile,1-methyl-(9CI)
  • 1-Methyl-1H-benzimidazole-2-acetonitrile
  • 1-Methyl-2-(cyanomethyl)-1H-benzoimidazole
  • (1-Methyl-1H-benzoimidazol-2-yl)acetonitrile
  • 2-(1-methylbenzimidazol-2-yl)acetonitrile
  • 2-(1-methylbenzimidazol-2-yl)ethanenitrile
  • 1-Methyl-2-benziMidazolylacetonitrile
  • 2-(1-Methyl-1H-benzo[d]iMidazol-2-yl)acetonitrile
CAS:
2735-62-8
MF:
C10H9N3
MW:
171.2
Product Categories:
  • BENZIMIDAZOLE
Mol File:
2735-62-8.mol
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(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
Appearance
Off-white to light brown Solid
EPA Substance Registry System
1-Methyl-2-benzimidazoleacetonitrile (2735-62-8)
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Safety Information

HS Code 
2933998090
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(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile Usage And Synthesis

Synthesis

4414-88-4

77-78-1

2735-62-8

The general procedure for the synthesis of 2-(1-methyl-1H-benzo[d]imidazol-2-yl)acetonitrile from 2-cyanomethylbenzimidazole and dimethyl sulfate was as follows: 1.2 equivalents of dimethyl sulfate was added drop-wise to a mixture containing benzimidazol-2-ylacetonitrile (3b) and 1.1 equivalents of aqueous sodium hydroxide, and the temperature of the reaction was maintained at 30 °C, with continuous stirring for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and the precipitate was collected by filtration, washed several times with deionized water and subsequently dried. The yield of the final product was 78%.

References

[1] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 9, p. 2053 - 2059
[2] Synthetic Communications, 2007, vol. 37, # 13, p. 2259 - 2266
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 1, p. 238 - 252
[4] Angewandte Chemie - International Edition, 2014, vol. 53, # 27, p. 7079 - 7084
[5] Angew. Chem., 2014, vol. 126, # 27, p. 7199 - 7204,6

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