Boc-p-amino-D-Phe(Fmoc)-OH, with the CAS number 173054-11-0, is a protected amino acid derivative commonly used in peptide synthesis. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which is often employed to protect the amino group during chemical reactions. The presence of the Fmoc (9-fluorenylmethoxycarbonyl) group indicates that it is also protected at the amino position, allowing for selective deprotection under mild conditions. The "p-amino" designation refers to the para-amino substitution on the phenyl ring of the phenylalanine residue, which can influence the compound's reactivity and interactions. This amino acid derivative is particularly valuable in solid-phase peptide synthesis, where the protection and deprotection strategies are crucial for the successful assembly of peptides. Its structural characteristics contribute to its utility in the development of peptide-based therapeutics and research applications in biochemistry and medicinal chemistry. Overall, Boc-p-amino-D-Phe(Fmoc)-OH is a versatile building block in the synthesis of complex peptides.

Boc-p-amino-D-Phe(Fmoc)-OH

173054-11-0: Boc-D-Phe(4-NHFmoc)-OH, Boc-D-4-Aminophenylalanine(Fmoc)

BOC-D-PHE(4-NHFMOC)-OH

Boc-D-(4-Fmoc)-Aminophenylalanine

(R)-3-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid

Boc-D-(4-Fmoc)-aminophenylalanine

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CAS 173054-11-0: Boc-p-amino-D-Phe(Fmoc)-OH

BOC-D-PHE(4-NHFMOC)-OH

Ref: IN-DA00APPD

Boc-D-(4-Fmoc)-Aminophenylalanine

Ref: 10-F021377

(R)-3-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid

Ref: 54-OR75944

(R)-3-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid

Ref: 10-F790860

Boc-D-(4-Fmoc)-aminophenylalanine

Ref: 7W-GM2888

Boc-4-(Fmoc-amino)-D-phenylalanine

Ref: 3D-FB47895