Chemical Properties of 6,6-dimethoxy-2,5,5-trimethylhex-2-ene (CAS 67674-46-8)

6,6-dimethoxy-2,5,5-trimethylhex-2-ene

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InChI
InChI=1S/C11H22O2/c1-9(2)7-8-11(3,4)10(12-5)13-6/h7,10H,8H2,1-6H3
InChI Key
RDHNTAXPFZIMDN-UHFFFAOYSA-N
Formula
C11H22O2
SMILES
COC(OC)C(C)(C)CC=C(C)C
Molecular Weight1
186.29
CAS
67674-46-8
Other Names
  • Amarocite
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Physical Properties

Property Value Unit Source
Δf -96.19 kJ/mol Joback Calculated Property
Δfgas -441.41 kJ/mol Joback Calculated Property
Δfus 14.58 kJ/mol Joback Calculated Property
Δvap 43.25 kJ/mol Joback Calculated Property
log10WS -2.82 Crippen Calculated Property
logPoct/wat 2.988 Crippen Calculated Property
McVol 173.290 ml/mol McGowan Calculated Property
Pc 2021.76 kPa Joback Calculated Property
Inp [1166.60; 1166.60]   Show Hide
Inp 1166.60 NIST
Inp 1166.60 NIST
Tboil 496.29 K Joback Calculated Property
Tc 681.55 K Joback Calculated Property
Tfus 226.57 K Joback Calculated Property
Vc 0.651 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [401.76; 492.23] J/mol×K [496.29; 681.55] Show Hide
Cp,gas 401.76 J/mol×K 496.29 Joback Calculated Property
Cp,gas 418.70 J/mol×K 527.17 Joback Calculated Property
Cp,gas 434.87 J/mol×K 558.04 Joback Calculated Property
Cp,gas 450.28 J/mol×K 588.92 Joback Calculated Property
Cp,gas 464.96 J/mol×K 619.80 Joback Calculated Property
Cp,gas 478.94 J/mol×K 650.67 Joback Calculated Property
Cp,gas 492.23 J/mol×K 681.55 Joback Calculated Property

Similar Compounds

1-carbomethoxy-1,4-dimethylcyclohex-3-ene. (.+/-.)-Lavandulol, methyl ether. 14-Hydroxy-«alpha»-humulene. Humulene epoxide III. 1-carbomethoxy-1,3-dimethylcyclohex-3-ene. Humulene 1,2-epoxide. Lavandulyl isobutyrate. 1-carbomethoxy-1-methyl-4-tert-butylcyclohex-3-ene. 1-carbomethoxy-1-methylcyclohex-3-ene. Italicen-12-yl 2-methylbutyrate. 10-epi-Italicen-12-yl 2-methylbutyrate. Lavandulyl acetate. 10-epi-Italicen-12-yl isobutyrate. Italicen-12-yl isobutyrate. Lavandulyl propionate.

Find more compounds similar to 6,6-dimethoxy-2,5,5-trimethylhex-2-ene.

Sources

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