Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate

Base Information

Chemical Name:Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate
CAS No.:2199-46-4
Molecular Formula:C10H15 N O2
Molecular Weight:181.235
Hs Code.:2933990090
NSC Number:15767
DSSTox Substance ID:DTXSID60176412
Nikkaji Number:J305.405E
Wikidata:Q83046748
Pharos Ligand ID:KGSPSAPH4KFF
ChEMBL ID:CHEMBL1701700
Mol file:2199-46-4.mol

Synonyms:2199-46-4;Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate;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;NSC15767;Maybridge1_001943;MLS000042963;SCHEMBL2565795;CHEMBL1701700;HMS547A07;DTXSID60176412;HMS2365M21;CAA19946;MFCD00051948;NSC 15767;NSC-15767;STK726990;AKOS005524469;2,3,4-Trimethyl-5-carbethoxy-pyrrole;SB63578;AS-67194;SMR000019390;CS-0320674;EU-0079419;FT-0626005;D95952;Ethyl3,4,5-trimethyl-1H-pyrrole-2-carboxylate;SR-01000500434;SR-01000500434-1;Pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester;5-Methyl-4-methyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester

Suppliers and Price of Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Alfa Aesar
Ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 98%
5g
$ 122.00

Alfa Aesar
Ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 98%
1g
$ 32.50

Total 19 raw suppliers

Chemical Property of Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate

Chemical Property:

Vapor Pressure:0.00129mmHg at 25°C
Melting Point:125-126°C
Boiling Point:298.1°Cat760mmHg
Flash Point:134.1°C
PSA：42.09000
Density:1.059g/cm³
LogP:2.11660
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:181.110278721
Heavy Atom Count:13
Complexity:193

Purity/Quality:

99% ^*data from raw suppliers

Ethyl 3,4,5-trimethylpyrrole-2-carboxylate, 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=C(C(=C(N1)C)C)C
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.

Technology Process of Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate

There total 4 articles about Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: