2061-74-7

Usage

Uses

Used in Pharmaceutical Industry:
(4aR,4bS,6aR,7R,9aS,9bS,11aR)-4a,6a-dimethyl-7-[(2R)-6-methylheptan-2-yl]tetradecahydroindeno[5,4-f]chromen-2(3H)-one is used as a potential pharmaceutical compound for its unique structure and properties. Its specific arrangement of atoms and functional groups may offer therapeutic benefits in the development of new drugs.
Used in Chemical Research:
This complex organic molecule is also used in chemical research to study its properties, reactivity, and potential interactions with other molecules. Understanding its behavior can contribute to the advancement of organic chemistry and the discovery of new applications.
Used in Material Science:
(4aR,4bS,6aR,7R,9aS,9bS,11aR)-4a,6a-dimethyl-7-[(2R)-6-methylheptan-2-yl]tetradecahydroindeno[5,4-f]chromen-2(3H)-one may have potential applications in material science, where its unique structure could be utilized to develop new materials with specific properties for various industries.

Upstream product

• 601-57-0 Cholest-4-en-3-one 
• 2672-41-5 4-oxa-5α-cholestane 
• 6908-02-7 3-keto-A-nor-5α-cholestane 
• 2061-75-8 4-oxa-5-cholesten-3-one 
• 83492-08-4 3-[(3R,3aR,5aS,6R,7R,9aS,9bS)-3-((R)-1,5-Dimethyl-hexyl)-7-hydroxy-3a,6-dimethyl-dodecahydro-cyclopenta[a]naphthalen-6-yl]-propionic acid 
• 1508-94-7 3,5-seco-4-nor-cholestan-5-one-3-oic acid 

Relevant academic research and scientific papers

Expedited Baeyer-Villiger oxidation of steroidal ketones by microwave irradiation

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.

Ceric ammonium nitrate (CAN) catalyzed Baeyer-Villiger oxidation of carbonyl compounds, specially 20-oxosteroids

The role of ceric ammonium nitrate (CAN) as an effective catalyst in the peracid induced Baeyer-Villiger oxidation of carbonyl compounds with special reference to steroids has been demonstrated.

Stereochemical studies. XI. Equilibria between δ-hydroxy-acids and δ-lactones in aqueous tetrahydrofuran. Relative stabilities of isomeric δ-lactones

The equilibrium constants K' for the hydrolysis of 13 δ-lactones to hydroxy-acids in 54percent (mol/mol) aqueous tetrahydrofuran at 25 deg C have been determined.The equilibrium constants for the isomerization of the five δ-lactones into their epimers, and for the isomerization of their hydroxy-acids into their epimers, have been calculated by the methods of conformational analysis.These calculated values are consistent with the experimental values of K'.Addition of methyl groups to a hydroxy-acid decreases K' (the Thorpe-Ingold effect).