76043-47-5 Usage
Description
(5aS,5bS,7aS,8S,10aS,10bR,12aS)-5a,7a-dimethyl-2-oxohexadecahydro-2H-cyclopenta[5,6]naphtho[1,2-d]oxepin-8-yl acetate is a complex organic molecule characterized by its intricate chemical structure. It consists of a cyclopentane ring, a naphthalene ring, and an oxepin ring, along with an acetate group. This unique arrangement of carbon, hydrogen, and oxygen atoms in specific patterns suggests that the compound may have distinct pharmacological or biochemical properties. Further research and analysis are required to fully comprehend its characteristics and potential applications.
Uses
Used in Pharmaceutical Industry:
(5aS,5bS,7aS,8S,10aS,10bR,12aS)-5a,7a-dimethyl-2-oxohexadecahydro-2H-cyclopenta[5,6]naphtho[1,2-d]oxepin-8-yl acetate is used as a potential pharmaceutical compound for its unique structure and possible pharmacological or biochemical properties. The specific application reason would depend on the results of further research and analysis, which may reveal its potential therapeutic effects or interactions with biological systems.
Used in Chemical Research:
(5aS,5bS,7aS,8S,10aS,10bR,12aS)-5a,7a-dimethyl-2-oxohexadecahydro-2H-cyclopenta[5,6]naphtho[1,2-d]oxepin-8-yl acetate is used as a subject of study in chemical research to understand its properties, reactivity, and potential applications in various fields. (5aS,5bS,7aS,8S,10aS,10bR,12aS)-5a,7a-dimethyl-2-oxohexadecahydro-2H-cyclopenta[5,6]naphtho[1,2-d]oxepin-8-yl acetate's unique structure may provide insights into new chemical reactions or mechanisms, contributing to the advancement of chemical science.
Check Digit Verification of cas no
The CAS Registry Mumber 76043-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,4 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76043-47:
(7*7)+(6*6)+(5*0)+(4*4)+(3*3)+(2*4)+(1*7)=125
125 % 10 = 5
So 76043-47-5 is a valid CAS Registry Number.
76043-47-5Relevant articles and documents
Expedited Baeyer-Villiger oxidation of steroidal ketones by microwave irradiation
Borah, Juri Moni,Chowdhury, Pritish
experimental part, p. 1341 - 1345 (2011/11/06)
Microwave (MW) assisted reactions are currently having considerable importance in the synthesis of organic compounds. Considering the remarkable application of Baeyer-Villiger (BV) reaction in the synthesis of natural products and steroid-peptide conjugates, we report here some of our findings of BV oxidation of carbonyl compounds with special reference to steroidal ketones under MW irradiation justifying its accelerating effect.
Resolution of conflicting migratory reports in ring expansion of 3-keto steroids to oxygen and nitrogen
Dave, Vinod,Stothers, J. B.,Warnhoff, E. W.
, p. 2666 - 2678 (2007/10/02)
The migration of C-2 and/or C-4 to O or N in the Beckmann, Schmidt, and Baeyer-Villiger reactions of 3-keto steroids has been studied with the aid of (13)Cmr spectroscopy.Authentic specimens of the eight possible lactone and lactam products from both 5α- and 5β-cholestan-3-one have been prepared; their physical properties and 13Cmr assignments are given.Seven ring expansion reactions reported to give only one product have been found to give both possible migration products.The much studied reactions of 5α-cholestan-3,6-dione and its derivatives have been reexamined.The results emphasize again the necessity of using 13C spectra both as an analytical tool and as the best criterion of purity in work with these molecules.
