1433975-21-3

Basic information

• Product Name: FMoc-D-4-Aph(tBu-CbM)-OH
• Synonyms: FMoc-D-4-Aph(tBu-CbM)-OH;4-[[[(1,1-Dimethylethyl)amino]carbonyl]amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine;(9H-Fluoren-9-yl)MethOxy]Carbonyl D-Aph(tBuCbm)-OH
• CAS NO: 1433975-21-3
• Molecular Formula: C29H31N3O5
• Molecular Weight: 501.57354
• EINECS: -0
• Mol File: 1433975-21-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: FMoc-D-4-Aph(tBu-CbM)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: FMoc-D-4-Aph(tBu-CbM)-OH(1433975-21-3)
• EPA Substance Registry System: FMoc-D-4-Aph(tBu-CbM)-OH(1433975-21-3)

Safety Data

• Hazardous Substances Data: 1433975-21-3(Hazardous Substances Data)

Usage

General Description

FMoc-D-4-Aph(tBu-CbM)-OH is a chemical compound that consists of a 9-fluorenylmethoxycarbonyl (FMoc) protected D-4-amino phenylalanine (4-Aph) with tert-butyl (tBu) and carboxybenzyl (CbM) protection group at the amino and carboxyl terminus. It is commonly used in peptide synthesis as a building block to introduce the 4-Aph residue into peptides, enabling the modification of the peptide properties for various applications such as drug development, biochemical studies, and pharmaceutical research. FMoc-D-4-Aph(tBu-CbM)-OH is known for its stability and compatibility with solid-phase peptide synthesis techniques, making it a valuable tool for the creation of diverse peptide structures.