Chemical Properties of Guaiacyl tiglate

Guaiacyl tiglate

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InChI
InChI=1S/C12H14O3/c1-4-9(2)12(13)15-11-8-6-5-7-10(11)14-3/h4-8H,1-3H3/b9-4+
InChI Key
MNXOFCMTJXDHDP-RUDMXATFSA-N
Formula
C12H14O3
SMILES
CC=C(C)C(=O)Oc1ccccc1OC
Molecular Weight1
206.24
Sources

Physical Properties

Property Value Unit Source
Δf -114.31 kJ/mol Joback Calculated Property
Δfgas -335.54 kJ/mol Joback Calculated Property
Δfus 23.36 kJ/mol Joback Calculated Property
Δvap 56.85 kJ/mol Joback Calculated Property
logPoct/wat 2.57 Crippen Calculated Property
Pc 2581.96 kPa Joback Calculated Property
Tboil 608.37 K Joback Calculated Property
Tc 825.53 K Joback Calculated Property
Tfus 339.29 K Joback Calculated Property
Vc 0.62 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 398.54 J/mol×K 608.37 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 2
=C< 1
>C=O (nonring) 1
=CH- (ring) 4
=C< (ring) 2
=CH- 1
-CH3 3

Similar Compounds

Guaiacyl angelate. Fumaric acid, di(2-methoxyphenyl) ester. Pseudoisoeugenyl tiglate I. Pseudoisoeugenyl tiglate. Succinic acid, di(2-methoxyphenyl) ester. Glutaric acid, di(2-methoxyphenyl) ester. Guaiacyl hexanoate. p-Cresyl isotiglate. Fumaric acid, 2-methoxyphenyl 3-methylbut-2-en-1-yl ester. Pimelic acid, di(2-methoxyphenyl) ester. Glutaric acid, di(2-isopropoxyphenyl) ester. Glutaric acid, monochloride, 2-methoxyphenyl ester. Phenol, 2-methoxy-, acetate. Pyrocatechol diacetate. 2-Ethylbutyric acid, 2-isopropoxyphenyl ester.

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