Chemical Properties of 3,5-Heptadienol, 2-ethylidene-6-methyl, isomer # 1

3,5-Heptadienol, 2-ethylidene-6-methyl, isomer # 1

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InChI
InChI=1S/C10H16O/c1-4-10(8-11)7-5-6-9(2)3/h4-7,11H,8H2,1-3H3
InChI Key
FSTMFKMUZPMDAZ-UHFFFAOYSA-N
Formula
C10H16O
SMILES
CC=C(C=CC=C(C)C)CO
Molecular Weight1
152.23
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Physical Properties

Property Value Unit Source
Δf 120.06 kJ/mol Joback Calculated Property
Δfgas -69.88 kJ/mol Joback Calculated Property
Δfus 23.73 kJ/mol Joback Calculated Property
Δvap 54.57 kJ/mol Joback Calculated Property
log10WS -2.83 Crippen Calculated Property
logPoct/wat 2.447 Crippen Calculated Property
McVol 144.730 ml/mol McGowan Calculated Property
Pc 2712.67 kPa Joback Calculated Property
Inp 1195.00 NIST
Tboil 532.62 K Joback Calculated Property
Tc 717.13 K Joback Calculated Property
Tfus 220.12 K Joback Calculated Property
Vc 0.556 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [326.14; 390.80] J/mol×K [532.62; 717.13] Show Hide
Cp,gas 326.14 J/mol×K 532.62 Joback Calculated Property
Cp,gas 338.48 J/mol×K 563.37 Joback Calculated Property
Cp,gas 350.12 J/mol×K 594.12 Joback Calculated Property
Cp,gas 361.13 J/mol×K 624.87 Joback Calculated Property
Cp,gas 371.55 J/mol×K 655.62 Joback Calculated Property
Cp,gas 381.42 J/mol×K 686.38 Joback Calculated Property
Cp,gas 390.80 J/mol×K 717.13 Joback Calculated Property

Similar Compounds

3,5-Heptadienol, 2-ethylidene-6-methyl, isomer # 2. (2E,4E)-2,4-Dimethyl-2,4-hexadien-1-ol. 2,4-Dimethyl-2,4-hexadien-1-ol, not E,E, # 1. 2,4-Dimethyl-2,4-hexadien-1-ol, not E,E, # 2. allo- neo-Ocimene. 2,4,6-Octatriene, 2,6-dimethyl-, (E,Z)-. 2,6-Dimethyl-octa-2,4,6-triene, cis. (4Z,6e)-2,6-dimethyl-2,4,6-octatriene. trans-Alloocimene. (4Z,6z)-2,6-dimethyl-2,4,6-octatriene. 2,4,6-Octatriene, 2,6-dimethyl-. 3,5-Heptadienal, 2-ethylidene-6-methyl-. 1,5-Cyclohexadiene-1-methanol, 4-(1-methylethyl)-. Methyl dehydrogeraniate. Myrcen-8-ol.

Find more compounds similar to 3,5-Heptadienol, 2-ethylidene-6-methyl, isomer # 1.

Sources

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