Methyltestosterone | |
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Molecular structure via molpic based on CDK |
Conformer [] | |
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Conformer structure via JSmol |
Physical properties [] | |
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Molecular mass | 302.5 g/mol [1] |
Appearance | Crystals from hexane [1] |
Odor | Odorless [1] |
Melting point | 161-166 °C [1] |
Solubility | Soluble in alcohol, methanol, ether and other organic solvents; sparingly soluble in vegetable oil [1] |
Predicted LogP | 3.4 [1] |
Structural Identifiers [] | |
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Molecular formula | C20H30O2 [1] |
IUPAC name | (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one [1] |
SMILES | CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C)O)C [1] |
InChI | InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3/t15-,16+,17+,18+,19+,20+/m1/s1 [1] |
InChIKey | GCKMFJBGXUYNAG-HLXURNFRSA-N [1] |
Methyltestosterone
Methyltestosterone (also known as 17-Methyltestosterone, Metandren, Android, Testred, Androsan, Androsten, Mesterone, Virilon, Dumogran or Masenone) is a
Stereochemistry []
Methyltestosterone is a