177966-64-2
177966-64-2
Chemical Structure
Fmoc-D-Phe(4-F)-OH
- CAS No.: 177966-64-2
- Formula:C24H20FNO4
- Molecular Weight:405.42
IUPAC Name: (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-fluorophenyl)propanoic acid
InChIKey: IXUMACXMEZBPJG-JOCHJYFZSA-N
SMILES: O=C(O)[C@@H](CC1=CC=C(F)C=C1)NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O
Biological Activity: Fmoc-D-Phe(4-F)-OH is a phenylalanine derivative[1].
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Fmoc-D-Phe(4-F)-OH | 99.89% | Fmoc-D-Phe(4-F)-OH is a phenylalanine derivative. | ||||||||||||||||||||
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Fmoc-Phe(4-Cl)-OH | 99.81% | Fmoc-Phe(4-Cl)-OH is a phenylalanine derivative. | ||||||||||||||||||||
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Fmoc-Phe(4-F)-OH | 99.81% | Fmoc-Phe(4-F)-OH is a phenylalanine derivative. | ||||||||||||||||||||
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Fmoc-Tyr-OH | 99.70% | Fmoc-Tyr-OH is a tyrosine derivative. | ||||||||||||||||||||
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-chlorophenyl)propanoic acid | 98.0% | (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-chlorophenyl)propanoic acid is a phenylalanine derivative. | ||||||||||||||||||||
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Fmoc-Phe(4-NH2)-OH | 98.24% | Fmoc-Phe(4-NH2)-OH is a phenylalanine derivative. | ||||||||||||||||||||
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Fmoc-Phe(4-I)-OH | 99.48% | Fmoc-Phe(4-I)-OH is a phenylalanine derivative. | ||||||||||||||||||||
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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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Fmoc-D-Phe(4-I)-OH | Fmoc-D-Phe(4-I)-OH is a phenylalanine derivative. | |||||||||||||||||||||
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Fmoc-Phe(4-Me)-OH | 99.88% | Fmoc-Phe(4-Me)-OH is a phenylalanine derivative. | ||||||||||||||||||||
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(((9H-Fluoren-9-yl)methoxy)carbonyl)-D-tyrosine | 99.50% | (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-tyrosine is a tyrosine derivative. | ||||||||||||||||||||
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