77702-25-1 Usage
Description
17,17-Dimethyl-18-norandrosta-1,4,13-trien-3-one is an anabolic-androgenic steroid and a chemical derivative of Methandrostenolone (M226000). It is a synthetic compound that exhibits potent anabolic and androgenic properties, making it a valuable substance in various applications.
Uses
Used in Pharmaceutical Industry:
17,17-Dimethyl-18-norandrosta-1,4,13-trien-3-one is used as an anabolic-androgenic steroid for the treatment of conditions that require enhanced muscle growth and strength, such as muscle wasting diseases, osteoporosis, and other conditions that result in muscle atrophy.
Used in Sports and Fitness Industry:
17,17-Dimethyl-18-norandrosta-1,4,13-trien-3-one is used as a performance-enhancing drug by athletes and bodybuilders to improve their physical performance, increase muscle mass, and promote faster recovery from intense training sessions.
Used in Research and Development:
17,17-Dimethyl-18-norandrosta-1,4,13-trien-3-one is used as a research compound in the development of new drugs and therapies targeting muscle growth, strength, and overall athletic performance. Its anabolic and androgenic properties make it a valuable tool for understanding the mechanisms of muscle development and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 77702-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77702-25:
(7*7)+(6*7)+(5*7)+(4*0)+(3*2)+(2*2)+(1*5)=141
141 % 10 = 1
So 77702-25-1 is a valid CAS Registry Number.
77702-25-1Relevant articles and documents
METHANDROSTENOLONE. MECHANISM OF HYDROCHLORIC ACID INDUCED FLUORESCENCE.
TISHLER,BRODY
, p. 161 - 164 (1964)
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Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17α-methyl steroids: synthesis and rearrangement
Bi, Honggang,Masse, Robert,Just, George
, p. 306 - 312 (2007/10/02)
A simple and convenient method has been developed to prepare sulfates of anabolic 17β-hydroxy-17α-methyl steroids.The sulfates of methandienone, 17α-methyltestosterone, mestanolone, oxandrolone, and stanozolol were prepared.Different A-ring functions were not affected under the sulfation condition.The buffered hydrolyses of these sulfates provided the 17-epimers of the original steroids and 17,17-dimethyl-18-nor-13(14)-ene steroids, presumably via the 17-carbocations. Keywords: steroids, tertiary sulfates; 17α-methyl steroids; 17β-methyl steroids; 17,17-dimethyl-18-norandrost-13(14)-enes; NMR
