1217722-24-1

Basic information

• Product Name: FMoc-(R)-3-aMino-2-phenylpropanoic acid
• Synonyms: FMoc-(R)-3-aMino-2-phenylpropanoic acid;(R)-3-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-2-phenylpropanoic acid;(R)-3-(9H-Fluoren-9-ylmethoxycarbonylamino)-2-phenyl-propionic acid;(9H-Fluoren-9-yl)MethOxy]Carbonyl (R)-3-Amino-2-phenylpropanoic acid
• CAS NO: 1217722-24-1
• Molecular Formula: C24H21NO4
• Molecular Weight: 387.42784
• Mol File: 1217722-24-1.mol

Chemical Properties

• Boiling Point: 619.0±50.0 °C(Predicted)
• Appearance: /
• Density: 1.275±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.95±0.10(Predicted)
• CAS DataBase Reference: FMoc-(R)-3-aMino-2-phenylpropanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: FMoc-(R)-3-aMino-2-phenylpropanoic acid(1217722-24-1)
• EPA Substance Registry System: FMoc-(R)-3-aMino-2-phenylpropanoic acid(1217722-24-1)

Safety Data

• Hazardous Substances Data: 1217722-24-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
FMoc-(R)-3-amino-2-phenylpropanoic acid is used as a key component in the synthesis of peptide-based drugs for its ability to contribute to the formation of complex peptide structures. The FMoc protecting group allows for a controlled release of the amino acid, which is essential for the precise assembly of biologically active peptides.
Used in Research Applications:
In research settings, FMoc-(R)-3-amino-2-phenylpropanoic acid is utilized as a fundamental building block for the creation of novel peptides with potential therapeutic properties. Its chiral nature and the presence of the FMoc protecting group make it a versatile tool for exploring the structure-activity relationships in peptide chemistry.
Used in Drug Development:
FMoc-(R)-3-amino-2-phenylpropanoic acid is employed as a critical intermediate in the development of new pharmaceuticals, where its controlled release and chiral properties are harnessed to produce peptides with specific biological functions and activities, contributing to the advancement of medicinal chemistry.