Identification | Back Directory | [Name]
ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE | [CAS]
2199-46-4 | [Synonyms]
AT-51095 thyl 3,4,5-trimethylpyrrole-2-carboxylate ETHYL 3,4,5-TRIMETHYLPYRROLE-2-CARBOXYLATE Ethyl 3,4,5-Trimethyl-2-pyrrolecarboxylate Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate ETHYL 4-METHYL-3,5-DIMETHYLPYRROLE-2-CARBOXYLATE 3,4,5-Trimethylpyrrole-2-carboxylic acid ethyl ester Pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester 3,4,5-TRIMETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER 1H-Pyrrole-2-carboxylicacid,3,4,5-trimethyl-,ethylester(9CI) 5-Methyl-4-methyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester | [Molecular Formula]
C10H15NO2 | [MDL Number]
MFCD00051948 | [MOL File]
2199-46-4.mol | [Molecular Weight]
181.23 |
Hazard Information | Back Directory | [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. |
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Energy Chemical
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