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CAS 13209-60-4

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(3β,17β)-3,17-Bis(acetyloxy)androst-5-en-7-one

Description:
(3β,17β)-3,17-Bis(acetyloxy)androst-5-en-7-one, commonly referred to as a synthetic steroid, is characterized by its structural features that include a steroid backbone with two acetoxy groups at the 3 and 17 positions. This compound is derived from androstane, a steroid framework, and exhibits properties typical of steroid hormones, such as potential biological activity and interaction with steroid receptors. The presence of the double bond at the 5 position and the ketone group at the 7 position contributes to its reactivity and stability. It is often utilized in biochemical research and pharmaceutical applications due to its ability to modulate various physiological processes. The acetoxy groups enhance its lipophilicity, facilitating membrane permeability and biological activity. As with many steroid derivatives, it may exhibit a range of effects on metabolism, growth, and reproduction, making it a subject of interest in both medicinal chemistry and endocrinology. Safety and handling precautions are essential due to its potential biological effects and the need for proper storage conditions to maintain stability.
Formula:C23H32O5
InChI:InChI=1S/C23H32O5/c1-13(24)27-16-7-9-22(3)15(11-16)12-19(26)21-17-5-6-20(28-14(2)25)23(17,4)10-8-18(21)22/h12,16-18,20-21H,5-11H2,1-4H3/t16-,17-,18-,20-,21-,22-,23-/m0/s1
InChI key:InChIKey=UCLVTARKINLGLA-GSLJADNHSA-N
SMILES:O=C1[C@@]2([C@@]([C@]3(C)C(=C1)C[C@@H](OC(C)=O)CC3)(CC[C@@]4(C)[C@]2(CC[C@@H]4OC(C)=O)[H])[H])[H]
Synonyms:
  • Androst-5-en-7-one, 3,17-bis(acetyloxy)-, (3β,17β)-
  • 3β,17β-Dihydroxyandrost-5-en-7-one diacetate
  • (3β,17β)-3,17-Bis(acetyloxy)androst-5-en-7-one
  • Androst-5-en-7-one, 3β,17β-dihydroxy-, diacetate
  • 3β,17β-Diacetoxyandrost-5-en-7-one
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