Home Chemistry Organic Building Blocks Aryls (8S,9S,14R)-1,2,6,7,8,9,10,11,12,13,14,15,16,17-Tetradecahydro-3H-Cyclopenta[A]Phenanthren-3-One
Reduction: ketones can be reduced to alcohols using reducing agents such as sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4). The ketone functional group in your compound can potentially be reduced to form an alcohol.
Oxidation: ketones can be oxidized to carboxylic acids using strong oxidizing agents like potassium permanganate (KMnO4) or chromic acid (H2CrO4).
Aldol Condensation: If you have two molecules of the compound, they can undergo an aldol condensation reaction to form a β-hydroxy ketone or β-hydroxy aldehyde, followed by further reactions to form a variety of products.
Nucleophilic Addition: Depending on the reaction conditions and the presence of other functional groups, nucleophiles (such as amines or hydrazines) can add to the ketone, leading to the formation of imines or hydrazones.
Grignard Reaction: If you have a compound with a suitable leaving group, it can react with a Grignard reagent to form a new carbon-carbon bond.
Halogenation: Under appropriate conditions, ketones can undergo halogenation reactions, where halogens (e.g., bromine or chlorine) can be added to the carbon atom adjacent to the carbonyl group.
Enolization: ketones can undergo enolization in the presence of strong bases, forming enols. Enols can further tautomerize to form keto-enol tautomers.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Carbon related+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :