1648-62-0 Usage
Description
(2beta,5alpha,17beta)-2-fluoro-3-oxoandrostan-17-yl acetate is a synthetic androgen, also known as an anabolic steroid, which is a derivative of the naturally occurring hormone testosterone. This chemical compound is characterized by its ability to mimic the effects of testosterone in the body, such as promoting muscle growth, increasing bone density, and enhancing physical performance. It is commonly used in the treatment of hormonal imbalances and certain medical conditions, including hypogonadism and delayed puberty.
Uses
Used in Medical Treatments:
(2beta,5alpha,17beta)-2-fluoro-3-oxoandrostan-17-yl acetate is used as a therapeutic agent for the treatment of hormonal imbalances and specific medical conditions such as hypogonadism and delayed puberty. It helps to restore normal hormone levels and alleviate symptoms associated with these conditions.
Used in Sports and Bodybuilding:
(2beta,5alpha,17beta)-2-fluoro-3-oxoandrostan-17-yl acetate is used as a performance-enhancing drug by athletes and bodybuilders. It is valued for its ability to improve muscle strength, endurance, and overall physical performance, making it a popular choice for those seeking to enhance their athletic abilities.
Used in Research:
This chemical compound is also used in scientific research to study the effects of androgens on the body and to develop new treatments for various medical conditions. Researchers use (2beta,5alpha,17beta)-2-fluoro-3-oxoandrostan-17-yl acetate to investigate the mechanisms of action of androgens and to explore potential applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 1648-62-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,4 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1648-62:
(6*1)+(5*6)+(4*4)+(3*8)+(2*6)+(1*2)=90
90 % 10 = 0
So 1648-62-0 is a valid CAS Registry Number.
1648-62-0Relevant articles and documents
Obtention d'α-fluorocetones par oxydation anodique de derives d'enol.
Laurent, E.,Marquet, B,Tardivel, R.,Thiebault, H.
, p. 955 - 964 (2007/10/02)
To obtain fluoroketones without the use of electrophilic fluorinating reagents, we have carried out the anodic oxidation of enol esters and enol ethers in acetonitrile/Et3N, 3HF solution.With enol esters the main product is a fluoroketone or an acetoxyketone respectively, depending on the structure of the starting compound.The enol ether cation-radicals seemed to be less reactive towards H2F3- ions than the corresponding enol ester ones.
α-FLUORINATION OF KETONES BY XENON AND IODOBENZENE DIFLUORIDES: A STEREOCHEMICAL EVIDENCE DEMONSTRATING THEIR MECHANISTIC DIFFERENCES
Tsushima, Tadahiko,Kawada, Kenji,Tsuji, Teruji
, p. 1165 - 1168 (2007/10/02)
Xenon difluoride reacts smoothly with various steroid silyl enol ethers in the absence of any acid catalyst to afford stereoselectively α-oriented α-fluoroketones in good yields while iodotoluene difluoride reacts rather sluggishly with these silyl enol ethers to competitively produce β-oriented α-fluoro ketones, elimination and other nucleophilic substitution products.The observed stereochemical contrast clearly suggest an electrophilic and nucleophilic mechanism for these reactions, respectively.