Home Chemistry Organic Building Blocks Aryls (8S,9S,14R)-7,8,9,11,12,13,14,15,16,17-Decahydro-6H-Cyclopenta[A]Phenanthrene
Hydrogenation: You can hydrogenate the compound to reduce any unsaturated bonds present, typically using a catalyst like palladium or platinum. This would result in the addition of hydrogen atoms to the double bonds, making the compound more saturated.
Oxidation: Depending on the specific functional groups present, you may be able to oxidize the compound to introduce oxygen atoms. Common oxidizing agents include potassium permanganate (KMnO4) or chromic acid (H2CrO4).
Substitution Reactions: If there are reactive functional groups such as halides, you can carry out substitution reactions. For example, you can perform nucleophilic substitution reactions with alkyl halides.
Aromatization: If the compound contains non-aromatic rings, you can attempt to aromatize them under certain conditions to convert them into aromatic rings.
Acid-Catalyzed Reactions: If the compound contains functional groups like alcohols or ethers, you can perform acid-catalyzed reactions such as dehydration to eliminate water and form double bonds.
Base-Catalyzed Reactions: If there are acidic protons, you can perform base-catalyzed reactions such as deprotonation or elimination reactions.
Reduction: Depending on the functional groups present, you can reduce specific groups using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Friedel-Crafts Reactions: If there are aromatic rings, you can perform Friedel-Crafts reactions, like acylation or alkylation, to introduce new substituents onto the aromatic ring.
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 :