Chemical Properties of Ethyl 3,4,5-trimethylpyrrole-2-carboxylate

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

InChI
InChI=1S/C10H15NO2/c1-5-13-10(12)9-7(3)6(2)8(4)11-9/h11H,5H2,1-4H3
InChI Key
WBOGFZDTCIQHSX-UHFFFAOYSA-N
Formula
C10H15NO2
SMILES
CCOC(=O)c1[nH]c(C)c(C)c1C
Molecular Weight1
181.24
Other Names
  • Ethyl 3,4,5-trimethyl-1H-pyrrole-2-carboxylate
  • Ethyl 3,4,5-trimethylpyrrole-2-carboxylate
  • Pyrrole-2-carboxylic acid, 3,4,5-trimethyl-, ethyl ester
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Physical Properties

Property Value Unit Source
ΔfH°gas -408.60 kJ/mol Relay (1.0) Calculated Property
ΔvapH° 74.26 kJ/mol Relay (1.0) Calculated Property
IE 7.71 eV NIST
log10WS -2.86 Relay (1.0) Calculated Property
logPoct/wat 1.635 Crippen Calculated Property
McVol 149.720 ml/mol McGowan Calculated Property
Pc 2483.51 kPa Relay (1.0-beta) Calculated Property
Tboil 541.64 K Relay (1.0) Calculated Property
Tfus 377.38 K Relay (1.0) Calculated Property

Cheméo can also estimate Critical Temperature, Critical Volume, Standard Gibbs free energy of formation, Acentric Factor for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Similar Compounds

1H-Pyrrole-2,4-dicarboxylic acid, 3,5-dimethyl-, diethyl ester. 1H-Pyrrole-2-carboxylic acid, 3,5-dimethyl-, ethyl ester. 3,5-dimethyl-4-propyl-1H-pyrrole-2-carboxylic acid ethyl ester. 1H-Pyrrole-2-carboxylic acid, 4,5-dimethyl-, ethyl ester. 1H-Pyrrole-2-carboxylic acid, 3,5-dimethyl-4-nitro-, ethyl ester. 2,4-Dimethyl-1H-pyrrole-5-carboxylic acid methyl ester. Pyrrole-3-carboxylic acid, 2,4,5-trimethyl-, ethyl ester. 1-Methyl-3-piperidyl cyclopentylphenylglycolate. Cytosine arabinoside, buto-oxime-TMS derivative. Dimetindene M (nor, OH), acetylated. 6H-Benzofuro[3a,3,2-ef][2]benzazepin-6-one, 4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-, (4aS,8aS)-. narwedine. Lycoramine. RTI 23. 1,3,5(10)-Oestratriene-2-methoxy-3,16«alpha»,17«beta»-triol, 3-TBDMS-16,17-PFP.

Find more compounds similar to Ethyl 3,4,5-trimethylpyrrole-2-carboxylate.

Sources

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