5941-92-4 Usage
Description
()-13-ethyl-3-methoxygona-1,3,5(10),8-tetraen-17-one is a synthetic organic compound that belongs to the class of steroids. It is a derivative of the hormone testosterone, known for its androgenic and anabolic properties, which make it useful in the development of muscle and bone tissue. This chemical compound is commonly used in the pharmaceutical industry for the synthesis of various hormones and pharmaceuticals and may have potential therapeutic applications in the treatment of certain medical conditions, although further research is needed to fully understand its effects and mechanisms of action.
Uses
Used in Pharmaceutical Industry:
()-13-ethyl-3-methoxygona-1,3,5(10),8-tetraen-17-one is used as a key intermediate in the synthesis of various hormones and pharmaceuticals for the treatment of different medical conditions. Its androgenic and anabolic properties make it a valuable component in the development of muscle and bone tissue.
Used in Hormone Replacement Therapy:
()-13-ethyl-3-methoxygona-1,3,5(10),8-tetraen-17-one is used as a hormone replacement therapy for conditions that require the administration of androgens or anabolic agents, such as hypogonadism and muscle wasting diseases.
Used in Sports and Bodybuilding:
()-13-ethyl-3-methoxygona-1,3,5(10),8-tetraen-17-one is used as a performance-enhancing substance by athletes and bodybuilders to improve muscle mass, strength, and physical performance. However, it is important to note that the use of this compound for such purposes may be prohibited by sports organizations and can have potential health risks.
Used in Research and Development:
()-13-ethyl-3-methoxygona-1,3,5(10),8-tetraen-17-one is used in research and development for the study of its potential therapeutic applications and mechanisms of action in the treatment of certain medical conditions. Further research is needed to fully understand its effects and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 5941-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,4 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5941-92:
(6*5)+(5*9)+(4*4)+(3*1)+(2*9)+(1*2)=114
114 % 10 = 4
So 5941-92-4 is a valid CAS Registry Number.
5941-92-4Relevant articles and documents
Total synthesis with a chirogenic opening move demonstrated on steroids with estrane or 18a-homoestrane skeleton
Quinkert,Del Grosso,Doring,Doring,Schenkel,Bauch,Dambacher,Bats,Zimmermann,Durner
, p. 1345 - 1391 (2007/10/02)
A concept of first choice for the synthesis of the title compounds had been proposed by Dane in the late 1930s. It was soon turned down, because the opening move - a chirogenic Diels-Alder reaction - did not work. With Lewis acids as mediators, however, a successful start has been achieved now. With Ti complexes of chelating ligands (Seebach's TADDOLs (= α,α,α',α'-tetraaryl-1,3-dioxolane-4,5-dimethanols)), enantioselective formation of the desired adducts does occur. Efficient total syntheses of 2 and 3a have been accomplished.
Synthesis of 13-alkyl-gon-4-ones
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, (2008/06/13)
The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.
