Chemical Properties of Myrtenyl methyl ether (CAS 202527-57-9)

Myrtenyl methyl ether

InChI
InChI=1S/C11H18O/c1-11(2)9-5-4-8(7-12-3)10(11)6-9/h4,9-10H,5-7H2,1-3H3
InChI Key
GMYAZJHVKQKHSD-UHFFFAOYSA-N
Formula
C11H18O
SMILES
COCC1=CCC2CC1C2(C)C
Molecular Weight1
166.26
CAS
202527-57-9
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Physical Properties

Property Value Unit Source
ω 0.3203 Relay (1.0) Calculated Property
Δf 53.27 kJ/mol Joback Calculated Property
Δfgas -163.55 kJ/mol Relay (1.0) Calculated Property
Δfus 15.21 kJ/mol Joback Calculated Property
Δvap 55.16 kJ/mol Relay (1.0) Calculated Property
IE 8.38 eV Relay (1.0) Calculated Property
log10WS -3.06 Relay (1.0) Calculated Property
logPoct/wat 2.625 Crippen Calculated Property
McVol 145.700 ml/mol McGowan Calculated Property
Pc 2568.89 kPa Joback Calculated Property
Inp 1160.50 NIST
I 1372.00 NIST
Tboil 475.51 K Relay (1.0) Calculated Property
Tc 715.67 K Relay (1.0) Calculated Property
Tfus 247.99 K Relay (1.0) Calculated Property
Vc 0.481 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [346.39; 439.22] J/mol×K [490.96; 695.76] Show Hide
Cp,gas 346.39 J/mol×K 490.96 Joback Calculated Property
Cp,gas 364.36 J/mol×K 525.09 Joback Calculated Property
Cp,gas 381.18 J/mol×K 559.23 Joback Calculated Property
Cp,gas 396.96 J/mol×K 593.36 Joback Calculated Property
Cp,gas 411.81 J/mol×K 627.49 Joback Calculated Property
Cp,gas 425.86 J/mol×K 661.62 Joback Calculated Property
Cp,gas 439.22 J/mol×K 695.76 Joback Calculated Property

Similar Compounds

Myrtenyl formate. (-)-Myrtenol, trifluoroacetate. Myrtenyl acetate. (6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl ethyl carbonate. Myrtenyl angelate. 2-pinen-10-yl isobutyrate. (-)-Myrtenol. Bicyclo[3.1.1]hept-2-ene-2-methanol, 6,6-dimethyl-. Bicyclo[3.1.1]hept-2-ene-2-methanol, 6,6-dimethyl-, (1S)-. myrtenyl 3-methylbutanoate. (-)-Myrtenol, trimethylsilyl ether. Glutaric acid, di(myrtenyl) ester. Myrtenyl laureate. Myrtenyl caprate. Myrtenyl hexanoate.

Find more compounds similar to Myrtenyl methyl ether.

Sources

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