3404-23-7 Usage
Uses
Used in Hormone-related Health Conditions:
(3beta,17beta)-androst-5-ene-3,17,19-triol is used as a potential therapeutic agent for hormone-related health conditions due to its role in the biosynthesis of steroid hormones such as testosterone and estrogen. It may help regulate hormone levels and alleviate symptoms associated with hormonal imbalances.
Used in Research and Medical Studies:
(3beta,17beta)-androst-5-ene-3,17,19-triol is used as a research compound to study its effects on the body's endocrine system. This helps scientists and medical professionals better understand the role of steroid hormones and their impact on various physiological processes.
Used in Synthesis of Biologically Active Molecules:
(3beta,17beta)-androst-5-ene-3,17,19-triol is used as a precursor in the synthesis of other biologically active molecules. Its unique structure and properties make it a valuable component in the development of new pharmaceuticals and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 3404-23-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3404-23:
(6*3)+(5*4)+(4*0)+(3*4)+(2*2)+(1*3)=57
57 % 10 = 7
So 3404-23-7 is a valid CAS Registry Number.
3404-23-7Relevant academic research and scientific papers
The hydroxylation of Δ5-androstenes by Cephalosporium aphidicola
Bensasson, Caroline M.,Hanson, James R.,Hunter, A. Christy
, p. 2355 - 2358 (2007/10/03)
Whereas the major hydroxylation product of 3β-hydroxy-5α-androstan- 17-one by Cephalosporium aphidicola is the 11α-alcohol, the presence of a Δ5-double bond in the substrate leads to non-stereospecific allylic hydroxylation at C-7. Hydroxylation at C-11 became a minor transformation and there was no detectable hydroxylation at C-14.
The Preparation and Dienone-Phenol Rearrangement of Androsta-2,5-diene-4,17-dione
Hanson, James R.,Raines, David,Knights, Steve G.
, p. 1311 - 1313 (2007/10/02)
The preparation of androsta-2,5-diene-4,17-dione from dehydroisoandrosterone is described.Its dienone-phenol rearrangement, in the presence of hydrobromic acid and glacial acetic acid, affords 1-methyl-4-hydroxy-estra-1,3,5(10)-trien-17-one.
