Chemical Properties of Borneol, carbamate

Borneol, carbamate

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InChI
InChI=1S/C11H19NO2/c1-10(2)7-4-5-11(10,3)8(6-7)14-9(12)13/h7-8H,4-6H2,1-3H3,(H2,12,13)
InChI Key
JFIIKUVKFMNHLU-UHFFFAOYSA-N
Formula
C11H19NO2
SMILES
CC1(C)C2CCC1(C)C(OC(N)=O)C2
Molecular Weight1
197.27
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Physical Properties

Property Value Unit Source
Δf -42.73 kJ/mol Joback Calculated Property
Δfgas -352.14 kJ/mol Joback Calculated Property
Δfus 15.95 kJ/mol Joback Calculated Property
Δvap 56.95 kJ/mol Joback Calculated Property
log10WS -2.88 Crippen Calculated Property
logPoct/wat 2.297 Crippen Calculated Property
McVol 161.550 ml/mol McGowan Calculated Property
Pc 2884.30 kPa Joback Calculated Property
Inp 1500.00 NIST
Tboil 608.79 K Joback Calculated Property
Tc 836.45 K Joback Calculated Property
Tfus 440.83 K Joback Calculated Property
Vc 0.605 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [454.44; 548.34] J/mol×K [608.79; 836.45] Show Hide
Cp,gas 454.44 J/mol×K 608.79 Joback Calculated Property
Cp,gas 471.63 J/mol×K 646.73 Joback Calculated Property
Cp,gas 487.87 J/mol×K 684.68 Joback Calculated Property
Cp,gas 503.41 J/mol×K 722.62 Joback Calculated Property
Cp,gas 518.50 J/mol×K 760.57 Joback Calculated Property
Cp,gas 533.39 J/mol×K 798.51 Joback Calculated Property
Cp,gas 548.34 J/mol×K 836.45 Joback Calculated Property

Similar Compounds

Isoborneol, carbamate. Isobornyl formate. Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, formate, endo-. Borneol, trifluoroacetate (ester). Acetic acid, 1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester. Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, acetate, (1S-endo)-. Isobornyl acetate. Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl, acetate. Bornyl acetate. Bornyl propanoate. Isobornyl propionate. Borneol, pentafluoropropionate. exo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl isobutyrate. Bornyl isobutyrate. 5-«beta»-Androstan-3-«alpha»,17-«alpha»-diol, TFA.

Find more compounds similar to Borneol, carbamate.

Sources

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