| Identification | Back Directory | [Name]
ETHYL 1-METHYL-5-NITROIMIDAZOLE-2-CARBOXYLATE | [CAS]
1564-49-4 | [Synonyms]
AKOS 92999 ETHYL 1-METHYL-5-NITROIMIDAZOLE-2-CARBOXYLATE Ethyl 1-Methyl-5-nitro-1H-iMidazole-2-carboxylate 1H-Imidazole-2-carboxylic acid, 1-methyl-5-nitro-, ethyl ester | [Molecular Formula]
C7H9N3O4 | [MDL Number]
MFCD03789116 | [MOL File]
1564-49-4.mol | [Molecular Weight]
199.16 |
| Chemical Properties | Back Directory | [Melting point ]
81-83°C | [Boiling point ]
350.7±34.0 °C(Predicted) | [density ]
1.42±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [pka]
-0.95±0.25(Predicted) | [Appearance]
White to off-white Solid |
| Hazard Information | Back Directory | [Synthesis]
Step 6a. ethyl 1-methyl-1H-imidazole-2-carboxylate (2.0 g, 13 mmol) was dissolved in 8 mL of concentrated H2SO4, followed by the slow addition of 8 mL of concentrated HNO3. The reaction mixture was stirred at 70 °C for 3 h. The reaction mixture was then extracted with dichloromethane (DCM). After completion of the reaction, the solution was diluted with H2O and the pH was adjusted to 7-8 with aqueous Na2CO3. The reaction mixture was extracted with dichloromethane (DCM) and the organic layers were combined and concentrated. Purification by silica gel column chromatography (eluent: ethyl acetate/petroleum ether) afforded the target compound 1-methyl-5-nitro-1H-imidazole-2-carboxylic acid ethyl ester as a yellow solid (0.9 g, 34.7% yield).ESI-MS m/z = 200.20 [M + H]+. | [References]
[1] Patent: WO2016/183266, 2016, A1. Location in patent: Page/Page column 50 |
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