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Ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 98%

CAS: 2199-46-4 | C10H15NO2 | 181.235 g/mol

$74.14 - $250.67

Chemical Identifiers

CAS 2199-46-4
Molecular Formula C10H15NO2
Molecular Weight (g/mol) 181.235
MDL Number MFCD00051948
InChI Key WBOGFZDTCIQHSX-UHFFFAOYSA-N
Synonym ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 1h-pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester, ethyl 3,4,5-trimethyl-2-pyrrolecarboxylate, 1h-pyrrole-2-carboxylic acid, 3,4,5-trimethyl, ethyl ester, acmc-20al0b, maybridge1_001943, 2,3,4-trimethyl-5-carbethoxy-pyrrole, 3,4,5-trimethylpyrrole-2-carboxylic acid ethyl ester, pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester, 1h-pyrrole-2-carboxylicacid, 3,4,5-trimethyl-, ethyl ester
PubChem CID 137479
IUPAC Name ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate
SMILES CCOC(=O)C1=C(C(=C(N1)C)C)C
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AAA1381403
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Thermo Scientific Chemicals
A1381403
1 g
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AAA1381406
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Thermo Scientific Chemicals
A1381406
5 g
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Description

Description

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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
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.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
Specifications

Chemical Identifiers

2199-46-4
181.235
WBOGFZDTCIQHSX-UHFFFAOYSA-N
137479
CCOC(=O)C1=C(C(=C(N1)C)C)C
C10H15NO2
MFCD00051948
ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 1h-pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester, ethyl 3,4,5-trimethyl-2-pyrrolecarboxylate, 1h-pyrrole-2-carboxylic acid, 3,4,5-trimethyl, ethyl ester, acmc-20al0b, maybridge1_001943, 2,3,4-trimethyl-5-carbethoxy-pyrrole, 3,4,5-trimethylpyrrole-2-carboxylic acid ethyl ester, pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester, 1h-pyrrole-2-carboxylicacid, 3,4,5-trimethyl-, ethyl ester
ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate

Specifications

2199-46-4
C10H15NO2
1 g
ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 1h-pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester, ethyl 3,4,5-trimethyl-2-pyrrolecarboxylate, 1h-pyrrole-2-carboxylic acid, 3,4,5-trimethyl, ethyl ester, acmc-20al0b, maybridge1_001943, 2,3,4-trimethyl-5-carbethoxy-pyrrole, 3,4,5-trimethylpyrrole-2-carboxylic acid ethyl ester, pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester, 1h-pyrrole-2-carboxylicacid, 3,4,5-trimethyl-, ethyl ester
CCOC(=O)C1=C(C(=C(N1)C)C)C
181.235
181.24
Ethyl 3,4,5-trimethylpyrrole-2-carboxylate
124°C to 128°C
MFCD00051948
132613
WBOGFZDTCIQHSX-UHFFFAOYSA-N
ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate
137479
98%
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Safety and Handling

Safety and Handling

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only