| Identification | Back Directory | [Name]
ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE | [CAS]
51605-32-4 | [Synonyms]
RARECHEM AL BI 0405
4-Carboethoxy-5-methylimidazole
4-Ethoxycarbonyl-5-methylimidazole
Ethyl 5-Methyl-4-imidazolecarboxylate
ETHYL 4-METHYL-5-IMIDAZOLECARBOXYLATE
ethyl 4-methylimidazole-5-carboxylate
Ethyl5-methyl-1H-4-imidazolecarboxylate
ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE
Ethyl 4-Methyl-5-iMidazolecarboxylate 98%
Ethyl 5-MethyliMidazole-4-carboxylate, 97%
ethyle4-methyl-5-imidazolecarboxylate, 98%
ETHYL 4-METHYL-5-IMIDAZOLECARBOXYLATE, 9 8%
ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLIC ACID
5-methyl-1h-imidazole-4-carboxylicaciethylester
1H-Imidazole-4-carboxylicacid,5-methyl-,ethylester
5-METHYL-1H-IMIDAZOLE-4-CARBOXYLIC ACID ETHYL ESTER
4-Methyl-1H-imidazole-5-carboxylic acid ethyl ester
5-Methyl-3H-imidazole-4-carboxylic acid ethyl ester
ethyl 4-Methyl-4,5-dihydro-1H-iMidazole-5-carboxylate
1H-Imidazole-5-carboxylic acid, 4-methyl-, ethyl ester | [EINECS(EC#)]
257-315-3 | [Molecular Formula]
C7H10N2O2 | [MDL Number]
MFCD00005199 | [MOL File]
51605-32-4.mol | [Molecular Weight]
154.17 |
| Chemical Properties | Back Directory | [Appearance]
off-white to yellow crystalline powder | [Melting point ]
204-206 °C(lit.)
| [Boiling point ]
323.7±22.0 °C(Predicted) | [density ]
1.171±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
chloroform/methanol: soluble50mg/mL, clear, colorless to light yellow | [form ]
Crystalline Powder or Crystals | [pka]
11.47±0.10(Predicted) | [color ]
Off-white to tan | [InChI]
InChI=1S/C7H10N2O2/c1-3-11-7(10)6-5(2)8-4-9-6/h4H,3H2,1-2H3,(H,8,9) | [InChIKey]
VLDUBDZWWNLZCU-UHFFFAOYSA-N | [SMILES]
C1NC(C(OCC)=O)=C(C)N=1 | [EPA Substance Registry System]
1H-Imidazole-4-carboxylic acid, 5-methyl-, ethyl ester (51605-32-4) |
| Hazard Information | Back Directory | [Chemical Properties]
off-white to yellow crystalline powder | [Uses]
Ethyl 4-methyl-5-imidazolecarboxylate forms coordination compounds with Co(2+). These compounds inhibit photosynthetic electron flow and ATP-synthesis and acts as Hill reaction inhibitors. | [General Description]
Ethyl 4-methyl-5-imidazolecarboxylate forms coordination compounds with Co(2+). These compounds inhibit photosynthetic electron flow and ATP-synthesis and acts as Hill reaction inhibitors. |
| Questions And Answer | Back Directory | [Application]
Ethyl 4-methyl-5-imidazolium carboxylate is an organic synthesis intermediate and a pharmaceutical intermediate that can be used in laboratory organic synthesis and pharmaceutical research and development, mainly as an intermediate for the active pharmaceutical ingredient cimetidine. |
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J & K SCIENTIFIC LTD.
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Energy Chemical
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Jia Xing Isenchem Co.,Ltd
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