855-22-1 Usage
Uses
Used in Medical Applications:
17beta-hydroxy-5alpha-androstan-3-one propionate is used as a hormone replacement therapy for conditions related to low testosterone levels. It helps to improve symptoms such as low sex drive, erectile dysfunction, and decreased energy levels by replacing or supplementing the natural testosterone in the body.
Used in Sports and Bodybuilding:
Testosterone propionate is used as a performance-enhancing drug in sports and bodybuilding. It is known for its anabolic effects, promoting muscle growth and strength, as well as improving physical performance. However, its use in this context is often controversial and may be subject to regulations and restrictions due to potential health risks and ethical concerns.
Used in Research and Development:
17beta-hydroxy-5alpha-androstan-3-one propionate is used as a research compound in the development of new pharmaceuticals and therapies targeting conditions related to hormonal imbalances, muscle wasting, and other health issues. Its properties and mechanisms of action provide valuable insights for the advancement of medical science and the creation of novel treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 855-22-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 855-22:
(5*8)+(4*5)+(3*5)+(2*2)+(1*2)=81
81 % 10 = 1
So 855-22-1 is a valid CAS Registry Number.
855-22-1Relevant academic research and scientific papers
Long-range effect of 17-substituents in 3-oxo steroids on 4,5-double bond hydrogenation
Sidova, Romana,Stransky, Karel,Kasal, Alexander,Slavikova, Barbora,Kohout, Ladislav
, p. 1528 - 1542 (2007/10/03)
The long-range effect of substituents in the 17-position on the hydrogenation of double bond of the steroidal Δ4-3-ketones in acetic acid on a platinum catalyst is described in a series of testosterone (1) and epitestosterone (5) esters with carboxylic acids of varying alkyl chain length. The ratio 5α-to 5β-products is affected by the nature of substituents in the position 17.
SYNTHESIS OF NEW ANTIATHEROMATOUS DRUGS. STUDY OF THE ESTERIFICATION OF 17β-HYDROXY-5α-ANDROSTAN-3-ONE
Volovel'skii, L. N.,Koryukina, V. N.,Popova, N. V.,Rastrepina, I. A.,Borozenets, L. K.
, p. 444 - 446 (2007/10/02)
The acylation of dihydrotestosterone with propionyl and p-chlorophenoxyisobutyryl chlorides leads to the formation of dihydrotestosterone esters and the 3-enol acylates of the dihydrotestosterone esters.The acid hydrolysis of the 3-enol acylates converts them into the coresponding dihydrotestosterone esters.
