Basic information Safety Supplier Related

METHYL 1-METHYL-4-NITRO-1H-IMIDAZOLE-2-CARBOXYLATE

Basic information Safety Supplier Related

METHYL 1-METHYL-4-NITRO-1H-IMIDAZOLE-2-CARBOXYLATE Basic information

Product Name:
METHYL 1-METHYL-4-NITRO-1H-IMIDAZOLE-2-CARBOXYLATE
Synonyms:
  • Methyl 4-nitro-1-methylimidazole-2-carboxylate
  • METHYL 1-METHYL-4-NITRO-1H-IMIDAZOLE-2-CARBOXYLATE
  • Methyl -methyl-4-nitro-1H-imidazole-2-carboxylate
  • Methyl 1-Methyl-4-nitroimidazole-2-carboxylate
  • 1H-Imidazole-2-carboxylic acid, 1-methyl-4-nitro-, methyl ester
  • 3-BROMO-10-CHLOROPHENOL
  • Carbamicacid,N-[2-(2-bromoethoxy)ethyl]-,1,6-dimethylethylester
  • Methyl 1-methyl-4-nitro-1H-imidazol-2-carboxylate
CAS:
169770-25-6
MF:
C6H7N3O4
MW:
185.14
Mol File:
169770-25-6.mol
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METHYL 1-METHYL-4-NITRO-1H-IMIDAZOLE-2-CARBOXYLATE Chemical Properties

Melting point:
157-158 °C
Boiling point:
345.0±34.0 °C(Predicted)
Density 
1.49±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-2.47±0.60(Predicted)
Appearance
White to off-white Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933299090
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METHYL 1-METHYL-4-NITRO-1H-IMIDAZOLE-2-CARBOXYLATE Usage And Synthesis

Synthesis

67-56-1

120095-64-9

169770-25-6

The general procedure for the synthesis of methyl 1-methyl-4-nitro-1H-imidazole-2-carboxylate from methanol and 2,2,2-trichloro-1-(1-methyl-4-nitro-1H-imidazol-2-yl)ethanone was as follows: methanol (40 mL) was added to a reaction flask containing 2,2,2-trichloro-1-(1-methyl-4-nitro-1H-imidazol-2-yl)ethanone, heated to 40 °C and stirred for 10 minutes. Subsequently, a small amount of sodium hydride (100 mg) was added to the reaction mixture to ensure complete methanolysis. After continued stirring for 2 h, the reaction mixture was filtered to afford methyl 1-methyl-4-nitro-1H-imidazole-2-carboxylate in 94% yield. The product was confirmed by 1H-NMR (CDCl3): δ 7.84 (s, 1H, Im-CH), 4.18 (s, 3H, CH3), 3.93 (s, 3H, CH3).EI-HRMS analysis resulted in a m/z calculated value of 185.0437 for C6H7N3O4 and a measured value of 185.0476 (100%).

References

[1] Patent: WO2007/45096, 2007, A1. Location in patent: Page/Page column 45; 86
[2] Heterocycles, 1995, vol. 41, # 6, p. 1181 - 1196
[3] Synthetic Communications, 2004, vol. 34, # 9, p. 1609 - 1615

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