5 A-Chloro-6 B,19-epoxy-3 B-hydroxy-5 A-androstan-17-one, with the CAS number 13244-39-8, is a synthetic steroid compound that belongs to the class of androgens. This compound features a chlorinated structure, which contributes to its unique biological activity. The presence of the epoxy group indicates a cyclic ether formation, which can influence its reactivity and interaction with biological systems. The hydroxyl group at the 3 B position suggests potential for hydrogen bonding, affecting its solubility and pharmacokinetics. As an androgen, it may exhibit anabolic properties, making it of interest in both medicinal chemistry and performance enhancement contexts. The structural modifications, including the chlorine and epoxy groups, can significantly alter its affinity for androgen receptors and its metabolic stability. Overall, this compound exemplifies the complexity of steroid chemistry and its implications in biological systems, though specific applications and effects would depend on further empirical studies.

5 A-CHLORO-6 B,19-EPOXY-3 B -HYDROXY-5 A-ANDROSTAN-17-ONE

13244-39-8: 5 A-Chloro-6 B,19-epoxy-3 B-hydroxy-5 A-androstan-17-one, with the CAS number 13244-39-8, is a synthetic steroid compound that belongs to the class of androgens. This compound features a chlorinated structure, which contributes to its unique biological activity. The presence of the epoxy group indicates a cyclic ether formation, which can influence its reactivity and interaction with biological systems. The hydroxyl group at the 3 B position suggests potential for hydrogen bonding, affecting its solubility and pharmacokinetics. As an androgen, it may exhibit anabolic properties, making it of interest in both medicinal chemistry and performance enhancement contexts. The structural modifications, including the chlorine and epoxy groups, can significantly alter its affinity for androgen receptors and its metabolic stability. Overall, this compound exemplifies the complexity of steroid chemistry and its implications in biological systems, though specific applications and effects would depend on further empirical studies.

CAS 13244-39-8

5 A-CHLORO-6 B,19-EPOXY-3 B -HYDROXY-5 A-ANDROSTAN-17-ONE

(3S,5R,6R,8S,9S,10R,13S,14S)-5-Chloro-3-hydroxy-13-methyltetradecahydro-6,10-(epoxymethano)cyclopenta[a]phenanthren-17(1H)-one

Ref: ST-EA-CP-E75013