Chemical Properties of Myrtenyl laureate

Myrtenyl laureate

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InChI
InChI=1S/C22H38O2/c1-4-5-6-7-8-9-10-11-12-13-21(23)24-17-18-14-15-19-16-20(18)22(19,2)3/h14,19-20H,4-13,15-17H2,1-3H3
InChI Key
QOZRLWRYYCNZEX-UHFFFAOYSA-N
Formula
C22H38O2
SMILES
CCCCCCCCCCCC(=O)OCC1=CCC2CC1C2(C)C
Molecular Weight1
334.54
Sources

Physical Properties

Property Value Unit Source
Δf 16.97 kJ/mol Joback Calculated Property
Δfgas -561.56 kJ/mol Joback Calculated Property
Δfus 45.30 kJ/mol Joback Calculated Property
Δvap 73.21 kJ/mol Joback Calculated Property
logPoct/wat 6.44 Crippen Calculated Property
Pc 1136.73 kPa Joback Calculated Property
Tboil 796.51 K Joback Calculated Property
Tc 988.86 K Joback Calculated Property
Tfus 475.16 K Joback Calculated Property
Vc 1.18 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 976.94 J/mol×K 796.51 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
-CH3 3
=CH- (ring) 1
=C< (ring) 1
-CH2- 11
>C< (ring) 1
>C=O (nonring) 1
>CH- (ring) 2
-CH2- (ring) 2

Similar Compounds

Myrtenyl caprate. Myrtenyl hexanoate. Myrtenyl 3-methylvalerate. myrtenyl 3-methylbutanoate. Glutaric acid, di(myrtenyl) ester. 2-pinen-10-yl isobutyrate. Glutaric acid, myrtenyl 3-methylbut-2-en-1-yl ester. Myrtenyl 2-methyl butyrate. Glutaric acid, myrtenyl 8-chlorooctyl ester. Myrtenyl acetate. Glutaric acid, myrtenyl 2-ethylhexyl ester. Glutaric acid, myrtenyl cyclohexylmethyl ester. Glutaric acid, myrtenyl dec-2-yl ester. Glutaric acid, myrtenyl 3-methylbut-2-yl ester. Myrtenyl angelate.

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