Chemical Properties of N-Methylserotonin

N-Methylserotonin

InChI
InChI=1S/C11H14N2O/c1-12-5-4-8-7-13-11-3-2-9(14)6-10(8)11/h2-3,6-7,12-14H,4-5H2,1H3
InChI Key
ASUSBMNYRHGZIG-UHFFFAOYSA-N
Formula
C11H14N2O
SMILES
CNCCc1c[nH]c2ccc(O)cc12
Molecular Weight1
190.24
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Physical Properties

Property Value Unit Source
ω 0.7041 Relay (1.0) Calculated Property
Δf 145.24 kJ/mol Relay (1.0-beta) Calculated Property
Δfgas -23.37 kJ/mol Relay (1.0) Calculated Property
Δvap 105.94 kJ/mol Relay (1.0) Calculated Property
IE 7.55 eV Relay (1.0) Calculated Property
log10WS -1.24 Relay (1.0) Calculated Property
logPoct/wat 1.153 Crippen Calculated Property
McVol 152.760 ml/mol McGowan Calculated Property
Pc 3910.76 kPa Relay (1.0-beta) Calculated Property
Inp 2025.00 NIST
Tboil 636.51 K Relay (1.0) Calculated Property
Tc 906.60 K Relay (1.0) Calculated Property
Tfus 466.77 K Relay (1.0) Calculated Property
Vc 0.535 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

Bufotenine. N-Acetyl-5-hydroxytryptamine, trimethylsilyl ether. Melatonin. 1H-Indole-3-ethanamine, N-methyl-. Bufotenin, monoTMS. 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-. Bis(3-indolylethyl)amine. 5-Methoxytryptamine. 5-Hydroxytryptamine, DTFMB-TMS. Tryptophan, 5-hydroxy, TMS. Psilocin. N-Methylserotonin, diTMS. N,N-Dimethyltryptamine. 5-Hydroxytryptamine, methyl, 2-PFP. 5-Hydroxytryptophan, ethoxycarbonylated, TBDMS # 1.

Find more compounds similar to N-Methylserotonin.

Sources

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