2,3-Dihydroxypropyl (8R,9S,10R,14S)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl carbonate, with the CAS number 117635-12-8, is a synthetic organic compound that belongs to the class of steroid derivatives. This compound features a complex polycyclic structure, characterized by multiple chiral centers, which contributes to its specific stereochemistry and biological activity. The presence of hydroxyl groups indicates potential for hydrogen bonding, influencing its solubility and reactivity. The ethynyl group suggests that it may participate in various chemical reactions, including those typical of alkynes. As a carbonate, it may also exhibit properties related to esterification and reactivity with nucleophiles. This compound is likely to be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural similarities to steroid hormones. However, detailed studies on its pharmacokinetics, toxicity, and therapeutic applications would be necessary to fully understand its potential uses.

2,3-dihydroxypropyl (8R,9S,10R,14S)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl carbonate (non-preferred name)

117635-12-8: 2,3-Dihydroxypropyl (8R,9S,10R,14S)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl carbonate, with the CAS number 117635-12-8, is a synthetic organic compound that belongs to the class of steroid derivatives. This compound features a complex polycyclic structure, characterized by multiple chiral centers, which contributes to its specific stereochemistry and biological activity. The presence of hydroxyl groups indicates potential for hydrogen bonding, influencing its solubility and reactivity. The ethynyl group suggests that it may participate in various chemical reactions, including those typical of alkynes. As a carbonate, it may also exhibit properties related to esterification and reactivity with nucleophiles. This compound is likely to be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural similarities to steroid hormones. However, detailed studies on its pharmacokinetics, toxicity, and therapeutic applications would be necessary to fully understand its potential uses.

CAS 117635-12-8

2,3-dihydroxypropyl (8R,9S,10R,14S)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl carbonate (non-preferred name)