CAS 173054-11-0
:Boc-p-amino-D-Phe(Fmoc)-OH
Description:
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.
Formula:C2H30N2O6
Synonyms:- Boc-D-Phe(4-NHFmoc)-OH
- Boc-D-4-Aminophenylalanine(Fmoc)
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Found 5 products.
Boc-D-Phe(4-NHFmoc)-OH
CAS:Formula:C29H30N2O6Purity:98%Color and Shape:SolidMolecular weight:502.5583(R)-3-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid
CAS:(R)-3-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acidPurity:98%Molecular weight:502.56g/mol(R)-3-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid
CAS:Purity:98%Molecular weight:502.5669861Boc-D-(4-Fmoc)-Aminophenylalanine
CAS:Formula:C29H30N2O6Purity:97.0%Color and Shape:SolidMolecular weight:502.567



