Home Chemistry Organic Building Blocks Aryls (9H-Fluoren-9-Yl)Methyl Cyclohexylcarbamate
Amine Reactions: The amine group in the cyclohexylcarbamate can undergo various reactions, such as acylation reactions with acyl chlorides or anhydrides to form amides.
Reduction: The carbonyl group in the carbamate can be reduced to the corresponding alcohol using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Oxidation: The alcohol functionality in the compound can be oxidized to the corresponding carbonyl group using oxidizing agents like chromium(VI) compounds (e.g., CrO3), PCC (pyridinium chlorochromate), or other suitable reagents.
Grignard Reaction: The compound can react with Grignard reagents, where the Grignard reagent would add to the carbonyl carbon, resulting in the formation of a tertiary alcohol.
Nucleophilic Substitution: The compound can undergo nucleophilic substitution reactions at the carbon bearing the fluorenyl group, depending on the reagents and conditions.
Esterification: The alcohol group can undergo esterification reactions with carboxylic acids and acid catalysts to form esters.
Reductive Amination: If conditions are suitable, reductive amination reactions can be carried out with the amine group in the presence of reducing agents to produce secondary or tertiary amines.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Carbon related+−
Formula Weight+−
click to sign in and save
Fmoc-(1S,2S)-2-aminocyclohexane carboxylic acid
click to sign in and save
(9H-Fluoren-9-yl)methyl (trans-4-aminocyclohexyl)carbamate hydrochloride
click to sign in and save
(1R,2S)-2-(Fmoc-amino)-cyclohexanecarboxylic acid
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :