Chemical Properties of 7-ethyl-N-methylindole

7-ethyl-N-methylindole

InChI
InChI=1S/C11H13N/c1-3-9-5-4-6-10-7-8-12(2)11(9)10/h4-8H,3H2,1-2H3
InChI Key
PNBISRBPZVZDNJ-UHFFFAOYSA-N
Formula
C11H13N
SMILES
CCc1cccc2ccn(C)c12
Molecular Weight1
159.23
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Physical Properties

Property Value Unit Source
ω 0.4699 Relay (1.0) Calculated Property
Δfgas 94.84 kJ/mol Relay (1.0) Calculated Property
Δvap 69.66 kJ/mol Relay (1.0) Calculated Property
IE 7.44 eV Relay (1.0) Calculated Property
log10WS -2.74 Relay (1.0) Calculated Property
logPoct/wat 2.741 Crippen Calculated Property
McVol 136.910 ml/mol McGowan Calculated Property
Pc 3058.31 kPa Relay (1.0-beta) Calculated Property
Tboil 540.53 K Relay (1.0) Calculated Property
Tc 774.09 K Relay (1.0) Calculated Property
Tfus 278.77 K Relay (1.0) Calculated Property
Vc 0.523 m3/kmol Relay (1.0) Calculated Property

Cheméo can also estimate Standard Gibbs free energy of formation for this compound, but it falls outside the models' validated range, so it is not shown here. Open the prediction tool to compute it on demand.

Similar Compounds

diphenhydramine. Carbazole, tetrahydro-9-acetyl-. N-ethyl-tetrahydrocarbazole. Phenindamine M (nor), acetylated. 1,2,3,4-Tetrahydrocarbazole, N-trifluoroacetyl-. Phenindamine M (nor, OH), acetylated. N-propyl-tetrahydrocarbazole. 4-Nitro-3-carbethoxy-1,2,7-trimethylindole. LYSERGAMIDE. Metergoline. LSD. Lysergic acid N-(methylpropyl)amide. Mirtazapine-M (nor-) AC. 5-Methoxytryptophan, ethoxycarbonylated, TBDMS. 5-Hydroxytryptophan, ethoxycarbonylated, TBDMS # 1.

Find more compounds similar to 7-ethyl-N-methylindole.

Sources

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