Fmoc-(R)-3-Amino-3-(3-nitrophenyl)propionic Acid: Key to Advanced Peptide Synthesis

Unlock complex peptide structures and drive drug discovery with this essential chiral building block.

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Advantages You Gain

Precision in Peptide Assembly

Utilize the Fmoc protection strategy to achieve selective deprotection and efficient coupling, crucial for building intricate peptide chains with high purity.

Enabling Drug Development

The chiral nature and functionalizable nitrophenyl group of (R)-3-Amino-3-(3-nitrophenyl)propionic acid make it invaluable for synthesizing enantiomerically pure drug candidates with enhanced efficacy.

Versatile Chemical Modifications

The presence of the nitrophenyl group provides a convenient site for further chemical reactions, allowing chemists to tailor molecular structures for specific research objectives.

Key Applications

Peptide Synthesis

Serve as a crucial building block in solid-phase peptide synthesis (SPPS) for creating complex and high-purity peptides.

Drug Development

Incorporate into novel pharmaceutical compounds to enhance specificity and efficacy, aiding in the creation of targeted therapeutics.

Medicinal Chemistry

Facilitate structure-activity relationship studies by allowing systematic modifications of peptide structures and exploring new chemical entities.

Biochemistry Research

Aid in the synthesis of bioactive peptides used as research tools to understand biological pathways and develop diagnostic agents.