Search Thermo Fisher Scientific
Element Search
Structure SearchThermo Scientific Chemicals
Ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 98%, Thermo Scientific Chemicals
Catalog number: A13814.06
5 g, Each
Thermo Scientific Chemicals
Ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 98%, Thermo Scientific Chemicals
Catalog number: A13814.06
5 g, Each
Quantity
Catalog number: A13814.06
also known as A13814-06
Price (USD)
142.00
Each
Quantity
-
Have Questions?
Chemical Identifiers
CAS
2199-46-4
IUPAC Name
ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate
Molecular Formula
C10H15NO2
InChI Key
WBOGFZDTCIQHSX-UHFFFAOYSA-N
SMILES
CCOC(=O)C1=C(C)C(C)=C(C)N1
Specifications
Specification SheetForm
Crystals or powder or crystalline powder
Assay (GC)
≥97.5%
Appearance (Color)
Pale pink
Melting Point (clear melt)
123.0-130.0?C
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.
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.
RUO – Research Use Only
Figures
Documents & Downloads
Certificates
Search by lot number or partial lot number
Frequently asked questions (FAQs)
Citations & References
Search citations by name, author, journal title or abstract text