Chemical Properties of 24-epi-Castasterone

24-epi-Castasterone

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InChI
InChI=1S/C28H48O5/c1-14(2)15(3)25(32)26(33)16(4)18-7-8-19-17-11-22(29)21-12-23(30)24(31)13-28(21,6)20(17)9-10-27(18,19)5/h14-21,23-26,30-33H,7-13H2,1-6H3/t15-,16?,17?,18-,19?,20?,21-,23?,24?,25-,26-,27-,28-/m0/s1
InChI Key
VYUIKSFYFRVQLF-RXTMYEETSA-N
Formula
C28H48O5
SMILES
CC(C)C(C)C(O)C(O)C(C)C1CCC2C3CC(=O)C4CC(O)C(O)CC4(C)C3CCC12C
Molecular Weight1
464.68
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Physical Properties

Property Value Unit Source
Δf -364.22 kJ/mol Joback Calculated Property
Δfgas -1205.09 kJ/mol Joback Calculated Property
Δfus 41.32 kJ/mol Joback Calculated Property
Δvap 143.61 kJ/mol Joback Calculated Property
log10WS -5.49 Crippen Calculated Property
logPoct/wat 3.806 Crippen Calculated Property
McVol 386.990 ml/mol McGowan Calculated Property
Pc 1194.82 kPa Joback Calculated Property
Inp [3660.00; 3662.00]   Show Hide
Inp 3660.00 NIST
Inp 3662.00 NIST
Inp 3660.00 NIST
Tboil 1299.82 K Joback Calculated Property
Tc 1651.65 K Joback Calculated Property
Tfus 722.58 K Joback Calculated Property
Vc 1.435 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1798.92; 2341.09] J/mol×K [1299.82; 1651.65] Show Hide
Cp,gas 1798.92 J/mol×K 1299.82 Joback Calculated Property
Cp,gas 1867.66 J/mol×K 1358.46 Joback Calculated Property
Cp,gas 1943.52 J/mol×K 1417.10 Joback Calculated Property
Cp,gas 2027.64 J/mol×K 1475.74 Joback Calculated Property
Cp,gas 2121.18 J/mol×K 1534.38 Joback Calculated Property
Cp,gas 2225.28 J/mol×K 1593.01 Joback Calculated Property
Cp,gas 2341.09 J/mol×K 1651.65 Joback Calculated Property

Similar Compounds

Castasterone. 3«alpha»,17«alpha»,20«alpha»,21-tetrahydroxy-5«beta»-Pregnane-11-one. 3«alpha»,17«alpha»,20«beta»,21-tetrahydroxy-5«beta»-Pregnane-11-one. Allopregnane-7«alpha»,11«alpha»-diol-3,20-dione. Androstan-17-one, 3,11-dihydroxy-, (3«alpha»,5«beta»,11«beta»)-. Pregnane-3,20-dione, 11-hydroxy-, (5«alpha»,11«alpha»)-. hyocholic acid. 11Beta-hydroxy-5alpha-androstan-17-one. Calamenone. 11«beta»-hydroxy-androsterone, 3«alpha»,11«beta»-dihydroxy-5«alpha»-androstane-17-one. 11«beta»-hydroxy-etiocholanolone, 3«alpha»,11«beta»-dihydroxy-5«beta»-androstane-17-one. Cedrane diol. ent-Kaurenoic acid, 16,17-dlhydro, 7«alpha», 16«beta»,17-triol, Me. 4-Hydroxypiperitone. Androstan-3-one, (5alpha), 11beta,17beta-dihydroxy-17alpha-methyl-.

Find more compounds similar to 24-epi-Castasterone.

Sources

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