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| | ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE Basic information |
| Product Name: | ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE | | Synonyms: | 1H-Pyrrole-2-carboxylicacid,3,4,5-trimethyl-,ethylester(9CI);5-Methyl-4-methyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester;ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE;ETHYL 4-METHYL-3,5-DIMETHYLPYRROLE-2-CARBOXYLATE;3,4,5-Trimethylpyrrole-2-carboxylic acid ethyl ester;Ethyl 3,4,5-Trimethyl-2-pyrrolecarboxylate;Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate;Pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester | | CAS: | 2199-46-4 | | MF: | C10H15NO2 | | MW: | 181.23 | | EINECS: | | | Product Categories: | PYRROLE | | Mol File: | 2199-46-4.mol |  |
| | ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE Chemical Properties |
| Melting point | 125-126°C | | Boiling point | 298.1±35.0 °C(Predicted) | | density | 1.059±0.06 g/cm3(Predicted) | | pka | 16.57±0.50(Predicted) | | BRN | 132613 |
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ALFA
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| | ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE Usage And Synthesis |
| Uses | Octamethylporphyrin was readily obtained from ethyl 3,4,5-trimethylpyrrole-2-carboxylate. Steric control can be overridden by apparent electronic effect is demonstrated by the even bulkier pyrrole derivative, ethyl 3,4,5-trimethylpyrrole-2-carboxylate. The reaction with diazonium salts of theEthyl 3,4,5-trimethylpyrrole-2-carboxylatehas been examined in detail by chromatographic and spectroscopic methods. In the presence of a strong mineral acid, Ethyl 3,4,5-trimethylpyrrole-2-carboxylate reacts with p-nitrobenzenediazonium ions to give a red, chemically labile, azo dye. |
| | ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE Preparation Products And Raw materials |
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