Chemical Properties of Longicamphenylene

Longicamphenylene

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InChI
InChI=1S/C15H24O/c1-13(2)8-5-9-14(3)11-7-6-10(12(14)16)15(11,13)4/h10-11H,5-9H2,1-4H3
InChI Key
VMYWIJUHQAMXNC-UHFFFAOYSA-N
Formula
C15H24O
SMILES
CC12CCCC(C)(C)C3(C)C(CCC13)C2=O
Molecular Weight1
220.35
Other Names
  • Longicamphenylone
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Physical Properties

Property Value Unit Source
Δf 78.99 kJ/mol Joback Calculated Property
Δfgas -279.51 kJ/mol Joback Calculated Property
Δfus 7.57 kJ/mol Joback Calculated Property
Δvap 49.24 kJ/mol Joback Calculated Property
log10WS -3.86 Crippen Calculated Property
logPoct/wat 3.818 Crippen Calculated Property
McVol 191.200 ml/mol McGowan Calculated Property
Pc 2237.64 kPa Joback Calculated Property
Inp [1554.00; 1569.00]   Show Hide
Inp 1569.00 NIST
Inp 1559.00 NIST
Inp 1561.00 NIST
Inp 1554.00 NIST
Tboil 630.56 K Joback Calculated Property
Tc 875.45 K Joback Calculated Property
Tfus 437.03 K Joback Calculated Property
Vc 0.730 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [561.94; 693.14] J/mol×K [630.56; 875.45] Show Hide
Cp,gas 561.94 J/mol×K 630.56 Joback Calculated Property
Cp,gas 584.99 J/mol×K 671.37 Joback Calculated Property
Cp,gas 606.96 J/mol×K 712.19 Joback Calculated Property
Cp,gas 628.30 J/mol×K 753.00 Joback Calculated Property
Cp,gas 649.46 J/mol×K 793.82 Joback Calculated Property
Cp,gas 670.93 J/mol×K 834.63 Joback Calculated Property
Cp,gas 693.14 J/mol×K 875.45 Joback Calculated Property

Similar Compounds

Longicamphenylone. (+)-Longicamphenylone. Bicyclo[2.2.1]heptan-2-one, 3,3-dimethyl-. 15-nor-Prezizaan-7-one. Camphor. 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one. (+)-2-Bornanone. ( S)-camphor. Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-. Camphor. 6,6-Dimethyl-2-methylenebicyclo[2.2.1]heptan-3-one. Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1R)-. dl-Camphoroquinone. Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1S)-. Androstane, 3,17-dione, (5alpha), 2alpha-methyl-.

Find more compounds similar to Longicamphenylene.

Sources

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