Chemical Properties of Trans-androsterone, 4-chlorobutyrate

Trans-androsterone, 4-chlorobutyrate

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InChI
InChI=1S/C23H35ClO3/c1-22-11-9-16(27-21(26)4-3-13-24)14-15(22)5-6-17-18-7-8-20(25)23(18,2)12-10-19(17)22/h15-19H,3-14H2,1-2H3
InChI Key
CXIUHMPDEUPPPV-UHFFFAOYSA-N
Formula
C23H35ClO3
SMILES
CC12CCC3C(CCC4CC(OC(=O)CCCCl)CCC43C)C1CCC2=O
Molecular Weight1
394.98
Sources

Physical Properties

Property Value Unit Source
Δf -77.27 kJ/mol Joback Calculated Property
Δfgas -686.43 kJ/mol Joback Calculated Property
Δfus 34.48 kJ/mol Joback Calculated Property
Δvap 81.86 kJ/mol Joback Calculated Property
logPoct/wat 5.53 Crippen Calculated Property
Pc 1326.17 kPa Joback Calculated Property
Tboil 941.96 K Joback Calculated Property
Tc 1183.48 K Joback Calculated Property
Tfus 608.51 K Joback Calculated Property
Vc 1.18 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1142.21 J/mol×K 941.96 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
>C=O (ring) 1
-CH2- 3
-Cl 1
-CH3 2
>C< (ring) 2
>C=O (nonring) 1
>CH- (ring) 5
-CH2- (ring) 9

Similar Compounds

Etiocholan-3«alpha»-ol-17-one, butyrate. Trans-androsterone, butyrate. Etiocholan-3«alpha»-ol-17-one, hexanoate. Trans-androsterone, octanoate. Etiocholan-3«alpha»-ol-17-one, octanoate. Trans-androsterone, hexanoate. 3«alpha»-Propanoyloxy-5«alpha»-androstan-17-one. Trans-androsterone, propionate. Trans-androsterone, acetate. Etiocholan-3«alpha»-ol-17-one, acetate. Androsterone acetate. 5A-Pregnanolone palmitate. 5A-Pregnanolone myristate. Androstan-17-one, 3-(formyloxy)-, (3«alpha»,5«beta»)-. Trans-androsterone, formate.

Find more compounds similar to Trans-androsterone, 4-chlorobutyrate.

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