Chemical Properties of Loliolide (CAS 73410-02-3)

Loliolide

InChI
InChI=1S/C11H16O3/c1-10(2)5-7(12)6-11(3)8(10)4-9(13)14-11/h4,7,12H,5-6H2,1-3H3
InChI Key
XEVQXKKKAVVSMW-UHFFFAOYSA-N
Formula
C11H16O3
SMILES
CC1(C)CC(O)CC2(C)OC(=O)C=C12
Molecular Weight1
196.24
CAS
73410-02-3
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Physical Properties

Property Value Unit Source
Δfus 16.18 kJ/mol Joback Calculated Property
logPoct/wat 1.409 Crippen Calculated Property
McVol 153.140 ml/mol McGowan Calculated Property
Inp [1698.00; 1784.00]   Show Hide
Inp 1784.00 NIST
Inp 1698.00 NIST
Inp 1784.00 NIST
Inp 1698.00 NIST

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Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [420.94; 493.34] J/mol×K [619.38; 823.83] Show Hide
Cp,gas 420.94 J/mol×K 619.38 Joback Calculated Property
Cp,gas 434.06 J/mol×K 653.45 Joback Calculated Property
Cp,gas 446.51 J/mol×K 687.53 Joback Calculated Property
Cp,gas 458.48 J/mol×K 721.60 Joback Calculated Property
Cp,gas 470.15 J/mol×K 755.68 Joback Calculated Property
Cp,gas 481.70 J/mol×K 789.75 Joback Calculated Property
Cp,gas 493.34 J/mol×K 823.83 Joback Calculated Property

Similar Compounds

isololiolide. Dihydroactinidioide. 2(4H)-benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-. 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (R)-. 5,8-epoxy-6-megastigmen-3,9-diol. 3,4-dihydro-3-hydroxyactinidol I. 3,4-dihydro-3-hydroxyactinidol II. 6Alpha,21-diacetoxy-11beta,17alpha-dihydroxypregn-4-ene-3,20-dione. GA6, MeTMS. Betamethasone dipropionate. T-2 Mycotoxin. Trichothec-9-ene-3,4,8,15-tetrol, 12,13-epoxy-, 15-acetate 8-(3-methylbutanoate), (3«alpha»,4«beta»,8«alpha»)-. GIBBERELLIC ACID. 3-epiGA1-13-O-«beta»-D-glucopyranoside, permethyl. GA8-13-O-glucoside, permethylated.

Find more compounds similar to Loliolide.

Sources

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