ChemicalBook--->CAS DataBase List--->2199-46-4

2199-46-4

2199-46-4 Structure

2199-46-4 Structure
IdentificationBack 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
Chemical PropertiesBack Directory
[Melting point ]

125-126°C
[BRN ]

132613
Safety DataBack Directory
[Safety Statements ]

24/25
Hazard InformationBack 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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