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| | ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE Basic information | | Application |
| | ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE Chemical Properties |
| 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) |
| Safety Statements | 24/25 | | WGK Germany | 3 | | TSCA | TSCA listed | | HS Code | 29332990 | | Storage Class | 11 - Combustible Solids |
| | ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE Usage And Synthesis |
| 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. | | 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. |
| | ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE Preparation Products And Raw materials |
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