Boc-(R)-3-Amino-4-(2-cyanophenyl)-butyric Acid: A Key Intermediate in Pharmaceutical and Peptide Synthesis

Unlock advanced therapeutic possibilities with this crucial chiral building block.

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Key Advantages

Advanced Chirality Control

The precise stereochemistry of this compound is crucial, offering chiral amino acid synthesis advantages for developing enantiomerically pure pharmaceuticals.

Enhanced Reactivity

The cyano group on the phenyl ring offers unique reactivity, useful in creating complex molecular structures for bioactive molecule design.

Protective Group Functionality

The Boc protecting group ensures controlled reactions in multi-step synthesis, vital for complex peptide structures in advanced peptide building blocks research.

Key Applications

Pharmaceutical Synthesis

Used as a critical intermediate in the development of drugs targeting neurological disorders, contributing to pharmaceutical intermediates for CNS disorders.

Peptide Synthesis

Serves as a chiral building block for creating therapeutic peptides with specific biological functions, a key aspect of advanced peptide building blocks.

Agrochemical Formulations

Acts as a building block in the creation of novel herbicides and pesticides, supporting enhanced agricultural productivity.

Research & Development

Essential for ongoing research in medicinal chemistry and drug discovery, supporting efforts in drug discovery intermediates.