Home Chemistry Organic Building Blocks Ketones (8S,14R)-6,7,8,9,10,11,12,13,14,15,16,17-Dodecahydro-3H-Cyclopenta[A]Phenanthren-3-One
Reduction: The ketone group can be reduced to an alcohol using reducing agents like sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Oxidation: The alcohol group can be oxidized back to a ketone or further oxidized to form other functional groups using oxidizing agents like potassium permanganate (KMnO4) or chromium(VI) reagents.
Esterification: The compound can undergo esterification reactions with carboxylic acids and suitable reagents, like acid chlorides or anhydrides, to form esters.
Alkylation: The compound may be susceptible to alkylation reactions, where alkyl groups are introduced to the molecule. This could involve the use of alkyl halides and strong bases.
Dehydration: Under certain conditions, dehydration reactions may occur, leading to the removal of water and the formation of double bonds.
Grignard Reaction: If there is a suitable electrophilic site, a Grignard reagent can be used to form new carbon-carbon bonds.
Hydrogenation: Unsaturated bonds, if present, can be reduced to saturated ones using hydrogen gas and a suitable catalyst like palladium on carbon (Pd/C).
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