Molecular structure of Fmoc-4-Amino-L-phenylalanine, CAS Number: 95753-56-3
Fmoc-4-Amino-L-phenylalanine (CAS 95753-56-3)
Alternate Names:
(2S)-3-(4-aminophenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid; Fmoc-L-Phe(4-NH2)-OH; Fmoc-p-amino-L-Phe-OH
Application:
Fmoc-4-Amino-L-phenylalanine is an aromatic amino acid derivative
CAS Number:
95753-56-3
Purity:
≥98%
Molecular Weight:
402.44
Molecular Formula:
C24H22N2O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Fmoc-4-Amino-L-phenylalanine (Fmoc-4-Phe) plays a role as a foundational component in both organic synthesis and peptide synthesis. It serves as a remarkably versatile and potent tool for creating peptides, proteins, and various other molecules. Essentially, Fmoc-4-Amino-L-phenylalanine is a derivative of an amino acid, characterized by a phenylalanine side chain accompanied by a 4-methoxycarbonyl (Fmoc) protecting group. This Fmoc group serves to safeguard the amino acid throughout the synthesis process and can be effortlessly removed whenever desired.
Fmoc-4-Amino-L-phenylalanine (CAS 95753-56-3) References
- In vitro selection of a photoresponsive peptide aptamer to glutathione-immobilized microbeads. | Tada, S., et al. 2015. J Biosci Bioeng. 119: 137-9. PMID: 25041711
- Fluorogenic Enhancement of an in Vitro-Selected Peptide Ligand by Replacement of a Fluorescent Group. | Wang, W., et al. 2016. Anal Chem. 88: 7991-7. PMID: 27459509
- Wash-free and selective imaging of epithelial cell adhesion molecule (EpCAM) expressing cells with fluorogenic peptide ligands. | K C, TB., et al. 2018. Biochem Biophys Res Commun. 500: 283-287. PMID: 29660346
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fmoc-4-Amino-L-phenylalanine, 1 g | sc-218526 | 1 g | $106.00 | |||
Fmoc-4-Amino-L-phenylalanine, 5 g | sc-218526A | 5 g | $428.00 |