39006-59-2 Usage
Uses
Used in Bodybuilding and Athletics:
(17beta)-17-methylandrost-4-en-3-one is used as a performance-enhancing drug for increasing muscle mass, strength, and performance in bodybuilders and athletes. Its high androgenic effects contribute to these benefits.
Used in Pharmaceutical Industry:
(17beta)-17-methylandrost-4-en-3-one is used as a research chemical in the development of pharmaceuticals targeting androgenic and anabolic effects. However, due to its potential side effects and health risks, its use in this industry is limited and strictly regulated.
Note: The use of (17beta)-17-methylandrost-4-en-3-one in competitive sports is prohibited due to its association with side effects and potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 39006-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39006-59:
(7*3)+(6*9)+(5*0)+(4*0)+(3*6)+(2*5)+(1*9)=112
112 % 10 = 2
So 39006-59-2 is a valid CAS Registry Number.
39006-59-2Relevant academic research and scientific papers
Zn-Mediated Hydrodeoxygenation of Tertiary Alkyl Oxalates
Ye, Yang,Ma, Guobin,Yao, Ken,Gong, Hegui
supporting information, p. 1625 - 1628 (2021/01/18)
Herein we describe a general, mild, and scalable method for hydrodeoxygenation of readily accessible tertiary alkyl oxalates by Zn/silane under Ni-catalyzed conditions. The reduction method is suitable for an array of structural motifs derived from tertiary alcohols that bear diverse functional groups, including the synthesis of a key intermediate en route to estrone.
Radical deoxygenation of hydroxyl groups via phosphites
Zhang, Liming,Koreeda, Masato
, p. 13190 - 13191 (2007/10/03)
A highly efficient, two-step sequence method for the deoxygenation of hydroxyl groups has been developed. The method involves the preparation of the 2-(2-iodophenyl)ethyl methyl phosphite derivative of an alcohol using methyl dichlorophosphite and 2-(2-iodophenyl)ethanol. Treatment of the phosphite intermediate with (n-Bu)3SnH/AIBN in refluxing benzene cleanly produces the deoxygenation product of the original alcohol. Copyright
