Home Life Science Amino Acids Amino Acid Derivatives (9H-Fluoren-9-Yl)Methyl (2-(Benzylthio)Ethyl)Carbamate
Amine Reactions: The amine group in the compound can participate in various reactions, such as acylation, alkylation, or condensation reactions.
Thiol Reactions: The benzylthio group can undergo reactions typical of thiol chemistry, including oxidation to form disulfides, substitution reactions, or reactions with electrophiles.
Protection/Deprotection: The fluorenyl group and carbamate moiety can be used for protection and deprotection strategies in organic synthesis.
Reduction: The carbonyl group in the compound can be reduced to the corresponding alcohol using reducing agents like LiAlH4 or NaBH4.
Substitution Reactions: The compound may undergo nucleophilic substitution reactions at various positions, depending on the reaction conditions and reagents.
Cleavage Reactions: The compound can potentially undergo cleavage reactions under specific conditions, such as cleavage of the carbamate or thioether bonds.
Functional Group Transformations: Various functional group transformations, including halogenation, oxidation, or reduction, can be applied to different parts of the molecule.
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