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Home/Compounds/Research Reagent/(2S)-3-[4-(AMINOMETHYL)PHENYL]-2-[(TERT-BUTOXY)CARBONYLAMINO]PROPANOIC ACID
C15H22N2O4
294.35 g/mol
Research Reagent

(2S)-3-[4-(AMINOMETHYL)PHENYL]-2-[(TERT-BUTOXY)CARBONYLAMINO]PROPANOIC ACID

CAS137452-49-4
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound

This compound is a protected amino acid derivative used as a research reagent in peptide synthesis. It features a tert-butoxycarbonyl (Boc) protecting group on the amino function and an aminomethyl substituent on the aromatic ring, making it suitable for building modified peptide chains.

Research compound for peptide synthesisBuilding block in solid-phase peptide synthesis

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

SimilarStructure SimilarSimilarity 0.78

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Boc-4-Iodo-L-phenylalanine

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Boc-O-tert-butyl-L-tyrosine

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SimilarStructure SimilarSimilarity 0.74

Boc-O-methyl-L-tyrosine

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pharmaceutical intermediate

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O-tert-butyl-L-serine

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research compound

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(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoic acid

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research compound

ApplicationSame Use

Fmoc-N-methyl-L-alloisoleucine

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research compound

Identifiers
IUPAC Name

(2S)-3-[4-(aminomethyl)phenyl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

InChIKey

SRHQPVLBHXDZGC-LBPRGKRZSA-N

SMILES

CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)CN)C(=O)O

Synonyms (12)
  • Boc-L-Phe(4-CH2NH2)-OH
  • Boc-p-(aminomethyl)-L-Phe-OH

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