Chemical Properties of 1-carbomethoxy-1-methyl-3-tert-butylcyclohex-3-ene

1-carbomethoxy-1-methyl-3-tert-butylcyclohex-3-ene

InChI
InChI=1S/C13H22O2/c1-12(2,3)10-7-6-8-13(4,9-10)11(14)15-5/h7H,6,8-9H2,1-5H3
InChI Key
LDNSZCYDGAYSFG-UHFFFAOYSA-N
Formula
C13H22O2
SMILES
COC(=O)C1(C)CCC=C(C(C)(C)C)C1
Molecular Weight1
210.31
Cheméo is a service of Céondo GmbH, since 2007, we provide simulation, modelling and software development services for the industry. Do not hesitate to contact us for your projects.

Physical Properties

Property Value Unit Source
Δfus 12.75 kJ/mol Joback Calculated Property
logPoct/wat 3.322 Crippen Calculated Property
McVol 186.310 ml/mol McGowan Calculated Property
I [1676.90; 1676.90]   Show Hide
I 1676.90 NIST
I 1676.90 NIST

Cheméo can also estimate Normal Boiling Point Temperature, Normal melting (fusion) point, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [480.52; 581.87] J/mol×K [575.96; 792.78] Show Hide
Cp,gas 480.52 J/mol×K 575.96 Joback Calculated Property
Cp,gas 500.11 J/mol×K 612.10 Joback Calculated Property
Cp,gas 518.45 J/mol×K 648.23 Joback Calculated Property
Cp,gas 535.67 J/mol×K 684.37 Joback Calculated Property
Cp,gas 551.89 J/mol×K 720.51 Joback Calculated Property
Cp,gas 567.25 J/mol×K 756.64 Joback Calculated Property
Cp,gas 581.87 J/mol×K 792.78 Joback Calculated Property

Similar Compounds

1-carbomethoxy-1-methyl-4-tert-butylcyclohex-3-ene. 1-carbomethoxy-1,3-dimethylcyclohex-3-ene. 1-carbomethoxy-1,4-dimethylcyclohex-3-ene. Olean-12-en-28-oic acid, 3-oxo-, methyl ester. 1-carbomethoxy-1-methylcyclohex-3-ene. Methyl abiet-7-en-18-oate. 1-carbomethoxy-3-methylcyclohex-3-ene. 1-Phenanthrenecarboxylic acid,7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a-7-trimethyl-, methyl ester. 1-Phenanthrenecarboxylic acid, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, methyl ester, [1R-(1«alpha»,4a«beta»,4b«alpha»,7«alpha»,10a«alpha»)]-. Methyl 7,15-Isopimaradien-18-oate. GA1 1,10-ene diacid, MeTMS. 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydro-1,4a-dimethyl-7-(1-methylethyl)-, methyl ester, [1R-(1«alpha»,4a«beta»,4b«alpha»,8a«beta»,10a«alpha»)]-. Methyl 13«beta»-Abieta-7,9(11)dien-18-oate. Methyl 8,15-Isopimaradien-18-oate. 1-Phenanthrenecarboxylic acid, 7-ethenyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydro-1,4a,7-trimethyl-, methyl ester, [1R-(1«alpha»,4a«beta»,7«beta»,10a«alpha»)]-.

Find more compounds similar to 1-carbomethoxy-1-methyl-3-tert-butylcyclohex-3-ene.

Sources

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.
These property values are available through the Cheméo API. A free account gives you an access key.