Basic information Safety Supplier Related

2-CYANO-N-METHYL-ACETAMIDE

Basic information Safety Supplier Related

2-CYANO-N-METHYL-ACETAMIDE Basic information

Product Name:
2-CYANO-N-METHYL-ACETAMIDE
Synonyms:
  • N1-METHYL-2-CYANOACETAMIDE
  • 2-Cyan-N-methyl-acetamide
  • 3-Oxo-3-(methylamino)propanenitrile
  • N-Methyl-2-cyanoacetamide
  • 2-CYANO-N-METHYL-ACETAMIDE
  • N-(Cyanoacetyl)methylamine
  • Acetamide, 2-cyano-N-methyl-
  • 4-bromo-N-propan-2-yl-1-pentanamine
CAS:
6330-25-2
MF:
C4H6N2O
MW:
98.1
EINECS:
228-705-0
Mol File:
6330-25-2.mol
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2-CYANO-N-METHYL-ACETAMIDE Chemical Properties

Melting point:
82 °C
Boiling point:
335.3±25.0 °C(Predicted)
Density 
1.044±0.06 g/cm3(Predicted)
vapor pressure 
0.009Pa at 25℃
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO, Methanol
form 
Solid
pka
5.44±0.10(Predicted)
color 
Pale Yellow
LogP
-1.96--0.445 at 25℃
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
20/21/22-36/37/38-22
Safety Statements 
22-26-36/37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2926907090
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2-CYANO-N-METHYL-ACETAMIDE Usage And Synthesis

Uses

2-Cyano-N-methylacetamide is used in the synthesis of pyridone compounds and benzimidazoles, for various pharmaceutical application.

Synthesis

105-56-6

74-89-5

6330-25-2

1. General procedure for the synthesis of 2-cyano-N-methylacetamide: 20 g (176.8 mmol) of ethyl cyanoacetate was added slowly and dropwise at 0 °C to a tetrahydrofuran (THF) solution of 10.9 g (353.6 mmol) of methylamine, which had been cooled to 0 °C. The reaction was completed with stirring. After the dropwise addition was completed, the reaction mixture was kept at 0 °C with continued stirring. Subsequently, the reaction mixture was stirred at room temperature overnight. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The crude product was purified by recrystallization with toluene to give 16.8 g of beige solid product in 96% yield with a melting point of 99 °C.

References

[1] Patent: US2011/251194, 2011, A1. Location in patent: Page/Page column 14
[2] Patent: US2011/124643, 2011, A1. Location in patent: Page/Page column 14
[3] Patent: US2013/178472, 2013, A1. Location in patent: Paragraph 0228
[4] Marine Drugs, 2012, vol. 10, # 6, p. 1412 - 1421
[5] Journal of Medicinal Chemistry, 2018, vol. 61, # 12, p. 5350 - 5366

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