2097-85-0 Usage
Uses
Used in Pharmaceutical Industry:
4,4-Dimethyl-5α-cholestan-3-one is used as an intermediate in the synthesis of cholesterol derivatives for various pharmaceutical applications. Its role in the production of 4α-Methyl-cholest-5-en-3β-ol (M295715) makes it a valuable compound in the development of drugs targeting cholesterol-related conditions.
Used in Research and Development:
4,4-Dimethyl-5α-cholestan-3-one is also utilized in research and development for studying the structure, function, and interactions of cholesterol and its derivatives in biological systems. Understanding the properties and behavior of 4,4-Dimethyl-5α-cholestan-3-one can contribute to the advancement of knowledge in the fields of biochemistry, cell biology, and pharmacology.
Used in the Production of Cholesterol Derivatives:
4,4-Dimethyl-5α-cholestan-3-one is used as a key component in the synthesis of various cholesterol derivatives, which have diverse applications in the pharmaceutical, chemical, and cosmetic industries. These derivatives can be used for the development of drugs targeting cholesterol-related diseases, as well as in the formulation of products for skin care and other cosmetic applications.
Used in the Study of Biological Membranes:
Due to its role in the synthesis of cholesterol, 4,4-Dimethyl-5α-cholestan-3-one is also used in the study of biological membranes, which are essential for maintaining cellular integrity and function. Research involving 4,4-Dimethyl-5α-cholestan-3-one can provide insights into the structure and dynamics of membrane lipids, which can be applied to the development of new therapeutic strategies and drug delivery systems.
Check Digit Verification of cas no
The CAS Registry Mumber 2097-85-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2097-85:
(6*2)+(5*0)+(4*9)+(3*7)+(2*8)+(1*5)=90
90 % 10 = 0
So 2097-85-0 is a valid CAS Registry Number.
2097-85-0Relevant academic research and scientific papers
CHROMIUMVI COMPLEX CATALYZED BENZYLIC OXIDATIONS IN THE PRESENCE OF TERT.BUTYL HYDROPEROXIDE
Muzart, Jacques
, p. 3139 - 3142 (2007/10/02)
In using t.BuOOH and a small quantity of 2,4-dimethylpentane-2,4-diol cyclic chromate, benzylic methylene groups are oxidised into carbonyl functions; t.butylperoxy compounds are postulated as intermediates.
The Photochemistry of α,β-Unsaturated Nitro Compounds and Nitronic Acids. Concerning Deconjugation and α,β-Unsaturated Ketone Formation
Grant, Richard D.,Pinhey, John T.,Rizzardo, Ezio,Smith, Geoffrey C.
, p. 1505 - 1519 (2007/10/02)
The photochemistry of cyclohexylidenenitromethane (6), 3-ethyl-2-nitropent-2-ene (7), (Z)-α-methyl-α'-nitrostilbene (12), (E)-3-methyl-1-nitro-1-phenylbut-1-ene (15) and 4,4-dimethyl-3-nitro-5α-cholest-2-ene (27) has been examined to determine the structural features required for deconjugation to the β,γ-unsaturated isomer.The mechanism of the light-induced formation of the corresponding α,β-unsaturated ketone, which may accompany deconjugation, has also been examined.Support for a scheme involving γ-hydrogen abstraction to give an unsaturated nitronic acid, followed by N-hydroxyoxaziridine formation and collapse to the ketone, is provided in the photochemistry of the stable nitronic acids, 4-t-butyl-aci-nitrocyclohexane (17) and 9-aci-nitrofluorene (18).Syntheses of the nitro olefins (6), (7), (12), (15) and (27), and the nitronic acid (17) are also reported.
