Chemical Properties of 1,3-Cyclobutanediol, 2,4-diethyl-2,4-dimethyl-, dipelargonate (CAS 105476-84-4)

1,3-Cyclobutanediol, 2,4-diethyl-2,4-dimethyl-, dipelargonate

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InChI
InChI=1S/C28H52O4/c1-7-11-13-15-17-19-21-23(29)31-25-27(5,9-3)26(28(25,6)10-4)32-24(30)22-20-18-16-14-12-8-2/h25-26H,7-22H2,1-6H3
InChI Key
YWIXAQMTRDSEPQ-UHFFFAOYSA-N
Formula
C28H52O4
SMILES
CCCCCCCCC(=O)OC1C(C)(CC)C(OC(=O)CCCCCCCC)C1(C)CC
Molecular Weight1
452.71
CAS
105476-84-4
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Physical Properties

Property Value Unit Source
ω 1.1042 Relay (... Calculated Property
Δf -268.42 kJ/mol Joback Calculated Property
Δfgas -1180.87 kJ/mol Relay (... Calculated Property
Δfus 60.50 kJ/mol Joback Calculated Property
Δvap 117.50 kJ/mol Relay (... Calculated Property
IE 9.06 eV Relay (... Calculated Property
log10WS -7.30 Relay (... Calculated Property
logPoct/wat 8.157 Crippen Calculated Property
McVol 409.400 ml/mol McGowan Calculated Property
Pc 743.26 kPa Joback Calculated Property
Tboil 642.87 K Relay (... Calculated Property
Tc 855.80 K Relay (... Calculated Property
Tfus 280.87 K Relay (... Calculated Property
Vc 1.510 m3/kmol Relay (... Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1486.88; 1681.54] J/mol×K [990.10; 1215.43] Show Hide
Cp,gas 1486.88 J/mol×K 990.10 Joback Calculated Property
Cp,gas 1517.96 J/mol×K 1027.66 Joback Calculated Property
Cp,gas 1549.26 J/mol×K 1065.21 Joback Calculated Property
Cp,gas 1581.02 J/mol×K 1102.77 Joback Calculated Property
Cp,gas 1613.48 J/mol×K 1140.32 Joback Calculated Property
Cp,gas 1646.91 J/mol×K 1177.88 Joback Calculated Property
Cp,gas 1681.54 J/mol×K 1215.43 Joback Calculated Property

Similar Compounds

1,3,5-Cyclohexanetriol, 2,2,4,4,6,6-hexamethyl-, tripelargonate. 1,3-Cyclobutanediol, 2,2,4,4-tetramethyl-, nonanoate, 2-ethylhexanoate. 1,3-Cyclobutanediol, 2,2,4,4-tetramethyl-, monopelargonate. 1,3-Cyclobutanediol, 2,2,4,4-tetramethyl-, monohexanoate. Nonanedioic acid, bis(8,8-dimethyl-2-oxabicyclo[4.2.0]octan-7-yl) ester. 1,3-Cyclobutanediol, 2,2,4,4-tetramethyl-, mono(2-ethylhexanoate). Bornyl hexanoate. Isobornyl laureate. Isobornyl caprate. Pentanoic acid, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester, endo-. 5«alpha»,17«alpha»-Dihydroepitestosterone octadecanoate. 5«beta»,17«beta»-Dihydrotestosterone tetradecanoate. 5«alpha»,17«beta»-Dihydrotestosterone heptanoate. 5«alpha»,17«beta»-Dihydrotestosterone decanoate. 5«beta»,17«alpha»-Dihydroepitestosterone decanoate.

Find more compounds similar to 1,3-Cyclobutanediol, 2,4-diethyl-2,4-dimethyl-, dipelargonate.

Sources

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