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Home/Compounds/Research Reagent/L-phenylalanine,(alphaS)-alpha-(((1,1-dimethylethoxy)carbonyl)amino)benzenebutanoyl-L-leucyl-,phenylmethylester
C37H47N3O6
629.8 g/mol
Research Reagent

L-phenylalanine,(alphaS)-alpha-(((1,1-dimethylethoxy)carbonyl)amino)benzenebutanoyl-L-leucyl-,phenylmethylester

CAS868540-15-2EC808-289-2
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound

This compound is a protected tripeptide derivative consisting of homophenylalanine, leucine, and phenylalanine residues with a benzyl ester terminus and a tert-butoxycarbonyl (Boc) protecting group. It is used as a research reagent in laboratory settings, primarily for peptide-related studies or as a synthetic intermediate.

research compoundsynthetic intermediate for peptide studies

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

StrongStructure SimilarSimilarity 0.85

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Referencesame scaffold

(S)-benzyl 2-((S)-2-((S)-2-amino-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoate 2,2,2-trifluoroacetate

CAS875309-83-4

research compound

Related Reading

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2026 has been a concentrated year for peptide therapeutics. Efficacy reached a new high in late-stage trials, the obesity field moved beyond the incretins to amylin, the oral route reached weight management, and peptide-guided radioligand therapy kept advancing — each point tied to a specific 2025–2026 result.

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Identifiers
IUPAC Name

benzyl (2S)-2-[[(2S)-4-methyl-2-[[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-phenylbutanoyl]amino]pentanoyl]amino]-3-phenylpropanoate

InChIKey

AKIABKDAWVWIHO-CPCREDONSA-N

SMILES

CC(C)C[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)OCC2=CC=CC=C2)NC(=O)[C@H](CCC3=CC=CC=C3)NC(=O)OC(C)(C)C

Synonyms (7)

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