Chemical Properties of Isobutylcarbamate, N-hexyl

Isobutylcarbamate, N-hexyl

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InChI
InChI=1S/C11H23NO2/c1-4-5-6-7-8-12-11(13)14-9-10(2)3/h10H,4-9H2,1-3H3,(H,12,13)
InChI Key
FTGWBFMEPQSPAF-UHFFFAOYSA-N
Formula
C11H23NO2
SMILES
CCCCCCNC(=O)OCC(C)C
Molecular Weight1
201.31
Sources

Physical Properties

Property Value Unit Source
Δf -105.23 kJ/mol Joback Calculated Property
Δfgas -466.98 kJ/mol Joback Calculated Property
Δfus 28.61 kJ/mol Joback Calculated Property
Δvap 55.28 kJ/mol Joback Calculated Property
logPoct/wat 2.95 Crippen Calculated Property
Pc 2053.03 kPa Joback Calculated Property
Tboil 577.10 K Joback Calculated Property
Tc 753.70 K Joback Calculated Property
Tfus 323.55 K Joback Calculated Property
Vc 0.70 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 470.14 J/mol×K 577.1 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
>CH- 1
-O- (nonring) 1
-CH3 3
-CH2- 6
>NH 1
>C=O (nonring) 1

Similar Compounds

1,6-Diaminohexane, bis-iso-BOC. 1,7-Diaminoheptane, bis-iso-BOC. Isobutylcarbamate, N-decyl. Isobutylcarbamate, N-butyl. Putrescine, bis-isoBOC. Isobutylcarbamate, N-isopentyl. Carbonic acid, monoamide, N-octadecyl-, octyl ester. Carbamic acid, butyl-, ethyl ester. Isobutylcarbamate, N,N-dihexyl. Piperidine, N-isoBOC. Hexyl carbamate. Isobutylcarbamate, N-pentyl. Pyrrolidine, N-isoBOC. Pentane, 1,5-bis-(methoxycarbonylamino). .GAMMA.-aminobutyric acid, n-isobutoxycarbonyl-, hexyl ester.

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