Chemical Properties of trans-Pinocarvyl formate

trans-Pinocarvyl formate

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InChI Key
Molecular Weight1

Physical Properties

Property Value Unit Source
Δf -21.21 kJ/mol Joback Calculated Property
Δfgas -289.93 kJ/mol Joback Calculated Property
Δfus 16.58 kJ/mol Joback Calculated Property
Δvap 47.60 kJ/mol Joback Calculated Property
logPoct/wat 2.15 Crippen Calculated Property
Pc 2673.54 kPa Joback Calculated Property
Tboil 529.97 K Joback Calculated Property
Tc 737.39 K Joback Calculated Property
Tfus 339.42 K Joback Calculated Property
Vc 0.57 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 371.07 J/mol×K 529.97 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
=CH2 1
=C< (ring) 1
O=CH- (aldehyde) 1
>C< (ring) 1
-CH3 2
>CH- (ring) 3
-CH2- (ring) 2

Similar Compounds

cis-Pinocarvyl acetate. trans-Pinocarvyl acetate. cis-Pinocarvyl acetate. (Z)-Pinocarvyl acetate. Pinocarvyl acetate. (-)-Marsupellol acetate. (-)-4-epi-Marsupellyl acetate. (-)-4-epi-Marsupellol acetate. Marsupellyl acetate. trans-Pinocarvyl laureate. trans-Pinocarvyl caprate. Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, [1S-(1«alpha»,3«alpha»,5«alpha»)]-. cis-Pinocarveol. Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-. Isopinocarveol.

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