1217655-36-1

Basic information

• Product Name: N-FMOC-3-(R)-AMINO-2-(R)-HYDROXY-3-NAPHTHALEN-2-YL-PROPIONIC ACID
• Synonyms: N-FMOC-3-(R)-AMINO-2-(R)-HYDROXY-3-NAPHTHALEN-2-YL-PROPIONIC ACID;(2R,3R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-hydroxy-3-(naphthalen-2-yl)propanoic acid
• CAS NO: 1217655-36-1
• Molecular Formula: C28H23NO5
• Molecular Weight: 453.49
• Mol File: 1217655-36-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N-FMOC-3-(R)-AMINO-2-(R)-HYDROXY-3-NAPHTHALEN-2-YL-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: N-FMOC-3-(R)-AMINO-2-(R)-HYDROXY-3-NAPHTHALEN-2-YL-PROPIONIC ACID(1217655-36-1)
• EPA Substance Registry System: N-FMOC-3-(R)-AMINO-2-(R)-HYDROXY-3-NAPHTHALEN-2-YL-PROPIONIC ACID(1217655-36-1)

Safety Data

• Hazardous Substances Data: 1217655-36-1(Hazardous Substances Data)

Usage

General Description

The chemical N-FMOC-3-(R)-amino-2-(R)-hydroxy-3-naphthalen-2-yl-propionic acid is a compound commonly used in the field of organic chemistry. It is a derivative of naphthalene and contains both an amino group and a hydroxy group, as well as a propionic acid moiety. The compound is often utilized as a building block for the synthesis of peptides and proteins, due to its ability to serve as a protected amino acid. It is often employed in the solid-phase peptide synthesis and has applications in the development of pharmaceuticals and biotechnology products. Additionally, the compound is commonly used as a fluorescent probe in biological research, due to its naphthalene-based structure which exhibits strong fluorescence properties.