missing translation for 'onlineSavingsMsg'
Learn More
  1. Home
  2. Products
  3. Chemicals
  4. Organic compounds
  5. Organic acids and derivatives
  6. Carboxylic acids and derivatives
  7. Monocarboxylic acids and derivatives
  8. Ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 98%

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

Catalog No. AAA1381403
Change view
Click to view available options
Quantity:
1 g
5 g
2 product options available for selection
Product selection table with 2 available options. Use arrow keys to navigate and Enter or Space to select.
Catalog No. Quantity
AAA1381403 1 g
AAA1381406 5 g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 2 options available.
2 options
Catalog No. AAA1381403 Supplier Thermo Scientific Chemicals Supplier No. A1381403
Only null left

Description

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

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.

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

Specifications

Melting Point 124°C to 128°C
Quantity 1 g
Beilstein 132613
Formula Weight 181.24
Percent Purity 98%
Chemical Name or Material Ethyl 3,4,5-trimethylpyrrole-2-carboxylate

Safety and Handling

TSCA No
Recommended Storage Ambient temperatures

RUO – Research Use Only