198561-04-5
Chemical Structure
Fmoc-Phe(4-Br)-OH
- CAS No.: 198561-04-5
- Formula:C24H20BrNO4
- Molecular Weight:466.32
IUPAC Name: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-bromophenyl)propanoic acid
InChIKey: TVBAVBWXRDHONF-QFIPXVFZSA-N
SMILES: O=C(O)[C@H](CC1=CC=C(Br)C=C1)NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O
Biological Activity: Fmoc-Phe(4-Br)-OH is a widely used amino acid derivative. Fmoc-Phe(4-Br)-OH can be used in the synthesis of compounds and for the study of protein-protein interactions and the development of biomaterials. Fmoc-Phe(4-Br)-OH can be used in peptide synthesis to incorporate phenylalanine bromide into the peptide chain[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fmoc-Phe(4-Br)-OH | 99.83% | Fmoc-Phe(4-Br)-OH is a widely used amino acid derivative. Fmoc-Phe(4-Br)-OH can be used in the synthesis of compounds and for the study of protein-protein interactions and the development of biomaterials. Fmoc-Phe(4-Br)-OH can be used in peptide synthesis to incorporate phenylalanine bromide into the peptide chain. | ||||||||||||||||||||
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- [1]. Qiao JX, et al. Synthesis of Fmoc-Protected Arylphenylalanines (Bip Derivatives) via Nonaqueous Suzuki-Miyaura Cross-Coupling Reactions. J Org Chem. 2016;81(19):9499-9506. [Content Brief]
- [2]. Wiedemeyer SJA, et al. Macrocyclic Inhibitors Targeting the Prime Site of the Fibrinolytic Serine Protease Plasmin. ChemMedChem. 2024;19(23):e202400360. [Content Brief]
Keywords
