1236-49-3 Usage
Description
5α-Androstan-17β-ol acetate, also known as a steroid ester, is a chemical compound derived from the steroid 5α-androstane. It is characterized by the presence of an acetoxy group at the 17th position, which distinguishes it from other steroid esters. This unique structure endows 5α-Androstan-17β-ol acetate with specific properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
5α-Androstan-17β-ol acetate is used as a pharmaceutical compound for its potential therapeutic effects. The expression is: 5α-Androstan-17β-ol acetate is used as a therapeutic agent for its steroidal properties and potential applications in treating various medical conditions.
Used in Research and Development:
In the field of research and development, 5α-Androstan-17β-ol acetate serves as a valuable chemical entity for studying the structure-activity relationships of steroidal compounds. The expression is: 5α-Androstan-17β-ol acetate is used as a research compound for understanding the effects of structural modifications on the biological activities of steroidal molecules.
Used in Cosmetics Industry:
5α-Androstan-17β-ol acetate may also find applications in the cosmetics industry, where it can be utilized for its potential benefits in skin care and anti-aging products. The expression is: 5α-Androstan-17β-ol acetate is used as an ingredient in the cosmetics industry for its potential skin care and anti-aging properties.
Used in Sports Nutrition:
In the sports nutrition industry, 5α-Androstan-17β-ol acetate could be used as a supplement to support muscle growth and recovery, taking advantage of its steroidal properties. The expression is: 5α-Androstan-17β-ol acetate is used as a sports supplement for its potential role in muscle growth and recovery.
Used in Chemical Synthesis:
5α-Androstan-17β-ol acetate can also be employed as a starting material or intermediate in the synthesis of other steroidal compounds with various applications. The expression is: 5α-Androstan-17β-ol acetate is used as a synthetic intermediate for the production of other steroidal compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1236-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1236-49:
(6*1)+(5*2)+(4*3)+(3*6)+(2*4)+(1*9)=63
63 % 10 = 3
So 1236-49-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H34O2/c1-14(22)23-19-10-9-17-16-8-7-15-6-4-5-12-20(15,2)18(16)11-13-21(17,19)3/h15-19H,4-13H2,1-3H3/t15-,16+,17+,18+,19+,20+,21+/m1/s1
1236-49-3Relevant articles and documents
Yamamura et al.
, p. 1049 (1967)
Expedited Baeyer-Villiger oxidation of steroidal ketones by microwave irradiation
Borah, Juri Moni,Chowdhury, Pritish
experimental part, p. 1341 - 1345 (2011/11/06)
Microwave (MW) assisted reactions are currently having considerable importance in the synthesis of organic compounds. Considering the remarkable application of Baeyer-Villiger (BV) reaction in the synthesis of natural products and steroid-peptide conjugates, we report here some of our findings of BV oxidation of carbonyl compounds with special reference to steroidal ketones under MW irradiation justifying its accelerating effect.
THE BIOTRANSFORMATION OF SOME STEROIDS BY CEPHALOSPORIUM APHIDICOLA
Hanson, James R.,Nasir, Habib
, p. 831 - 834 (2007/10/02)
Hydroxylation of 5α-androstane-3-one and 3,6-dione by C. aphidicla takes place at C-17β and, in the case of the latter, at C-5α.The fungus reduces 5α-androstan-17-one and the 3,17-dione to the 17β-alcohols. Key Word Index - Cephalosporium aphidicola; fungus; microbiological hydroxylation; steroids.
