Fmoc-7-amino-heptanoic acid serves as a versatile PROTAC linker with a terminal Fmoc-protected amine and carboxylic acid functionalities. It facilitates the synthesis of PROTACs by allowing the deprotection of the Fmoc group under basic conditions, yielding a free amine suitable for additional conjugation reactions. The carboxylic acid is reactive towards primary amines in the presence of coupling agents, enabling the formation of stable amide bonds essential for constructing complex molecular architectures in chemical research.
Fmoc-7-amino-heptanoic acid serves as a versatile PROTAC linker with a terminal Fmoc-protected amine and carboxylic acid functionalities. It facilitates the synthesis of PROTACs by allowing the deprotection of the Fmoc group under basic conditions, yielding a free amine suitable for additional conjugation reactions. The carboxylic acid is reactive towards primary amines in the presence of coupling agents, enabling the formation of stable amide bonds essential for constructing complex molecular architectures in chemical research.
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