Chemical Properties of Nandrolone (CAS 434-22-0)

Nandrolone

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InChI
InChI=1S/C18H26O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h10,13-17,20H,2-9H2,1H3/t13?,14?,15?,16?,17-,18?/m1/s1
InChI Key
NPAGDVCDWIYMMC-SVXFNXITSA-N
Formula
C18H26O2
SMILES
CC12CCC3C4CCC(=O)C=C4CCC3C1CCC2O
Molecular Weight1
274.40
CAS
434-22-0
Other Names
  • (+)-19-Nortestosterone
  • (17«beta»)-19-Nortestosterone
  • 17-Hydroxyestr-4-en-3-one
  • 17-«beta»-Hydroxyestr-4-en-3-one
  • 19-Norandrostenolone
  • 19-Nortestosterone
  • 19-Testosterone
  • 4-Estren-17«beta»-ol-3-one
  • Estr-4-en-3-one, 17-hydroxy-, (17«beta»)-
  • Estr-4-en-3-one, 17«beta»-hydroxy-
  • Menidrabol
  • NSC 3351
  • Nandrolon
  • Norandrostenolon
  • Norandrostenolone
  • Nortestonate
  • Nortestosterone
  • Oestrenolon
  • U 2410
Sources

Physical Properties

Property Value Unit Source
Δf 23.19 kJ/mol Joback Calculated Property
Δfgas -423.51 kJ/mol Joback Calculated Property
Δfus 24.69 kJ/mol Joback Calculated Property
Δvap 76.28 kJ/mol Joback Calculated Property
logPoct/wat 3.49 Crippen Calculated Property
Pc 2115.83 kPa Joback Calculated Property
Tboil 814.59 K Joback Calculated Property
Tc 1047.67 K Joback Calculated Property
Tfus 504.52 K Joback Calculated Property
Vc 0.84 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 782.94 J/mol×K 814.59 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
>C=O (ring) 1
=CH- (ring) 1
-OH (alcohol) 1
=C< (ring) 1
>C< (ring) 1
-CH3 1
>CH- (ring) 5
-CH2- (ring) 8

Similar Compounds

Androst-4-en-3-one, 17-hydroxy-, (17«alpha»)-. Testosterone. 17Alpha-methyl-beta-nortestosterone. Norethandrolone. 17-epi-Bolasterone. Calusterone. Bolasterone. 17-epi-Methyltestosterone. 17«alpha»-Methyltestosterone. Androsten-17-(beta)-ol-3-one, 17(alpha)-methyl-delta^4-. Methenolone. Spiro[cyclopropan-1,6'-testosterone]. Pregn-4-en-3-one, 20-hydroxy-, (20R)-. Pregn-4-en-3-one, 20-hydroxy-, (20S)-. Epitestosterone, methyl ether.

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