Chemical Properties of 1-Aminocyclopentanecarboxylic acid, N-(benzyloxycarbonyl)-, butyl ester

1-Aminocyclopentanecarboxylic acid, N-(benzyloxycarbonyl)-, butyl ester

InChI
InChI=1S/C18H25NO4/c1-2-3-13-22-16(20)18(11-7-8-12-18)19-17(21)23-14-15-9-5-4-6-10-15/h4-6,9-10H,2-3,7-8,11-14H2,1H3,(H,19,21)
InChI Key
CXNBXRAWINAMNA-UHFFFAOYSA-N
Formula
C18H25NO4
SMILES
CCCCOC(=O)C1(N=C(O)OCc2ccccc2)CCCC1
Molecular Weight1
319.40
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Physical Properties

Property Value Unit Source
ω 0.9365 Relay (1.0) Calculated Property
Δfgas -709.33 kJ/mol Relay (1.0) Calculated Property
Δvap 113.00 kJ/mol Relay (1.0) Calculated Property
log10WS -3.84 Relay (1.0) Calculated Property
logPoct/wat 3.773 Crippen Calculated Property
McVol 254.720 ml/mol McGowan Calculated Property
Pc 1721.73 kPa Joback Calculated Property
Tboil 631.39 K Relay (1.0) Calculated Property
Tc 885.24 K Relay (1.0) Calculated Property
Tfus 339.64 K Relay (1.0) Calculated Property
Vc 0.912 m3/kmol Relay (1.0) Calculated Property

Cheméo can also estimate Standard Gibbs free energy of formation, Ionization energy 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

1-Aminocyclopentanecarboxylic acid, N-(benzyloxycarbonyl)-, pentyl ester. 1-Aminocyclopentanecarboxylic acid, N-(benzyloxycarbonyl)-, heptyl ester. 1-Aminocyclopentanecarboxylic acid, N-(benzyloxycarbonyl)-, isohexyl ester. 1-Aminocyclopentanecarboxylic acid, N-(benzyloxycarbonyl)-, benzyl ester. Glycine, 2-cyclohexyl-N-benzyloxycarbonyl-, ethyl ester. Quebrachamine. SCHEMBL9488362. Lincomycin. Norhydrocodone. Adenosine, 2'-deoxy-N-(trimethylsilyl)-3'-O-(trimethylsilyl)-, 5'-[bis(trimethylsilyl) phosphate]. Morphinan-6-one, 4,5-epoxy-14-hydroxy-3-methoxy-, (5«alpha»)-. Oxymorphone, bis(trimethylsilyl) ether. Hydrocodone. Oxycodone. Morphinan-6-ol, 4,5-epoxy-3-methoxy-17-methyl-, (5«alpha»,6«alpha»)-.

Find more compounds similar to 1-Aminocyclopentanecarboxylic acid, N-(benzyloxycarbonyl)-, butyl ester.

Sources

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