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Home/Compounds/Research Reagent/N-Boc-N'-Fmoc-L-Lysine
C26H32N2O6
468.5 g/mol
Research ReagentWarning

(2S)-2-{[(tert-butoxy)carbonyl]amino}-6-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid

CAS84624-27-1EC966-532-9
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound

Boc-Lys(Fmoc)-OH is a protected lysine derivative commonly employed as a building block in solid-phase peptide synthesis. Its orthogonal protecting groups (Boc and Fmoc) allow selective deprotection during chain assembly, making it a standard reagent in research laboratories.

Peptide synthesis building blockResearch reagent for 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

StrongStructure SimilarSimilarity 0.94

N-Boc-N'-Fmoc-L-ornithine

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pharmaceutical intermediate

StrongStructure SimilarSimilarity 0.92

FMOC-D-Lys(BOC)-OH

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research compound

StrongStructure SimilarSimilarity 0.92

N-Fmoc-N'-Boc-L-Lysine

CAS71989-26-9

pharmaceutical intermediate

SimilarStructure SimilarSimilarity 0.80

N-Fmoc-N'-Boc-L-2,4-diaminobutyric acid

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pharmaceutical intermediate

ApplicationSame Use

Fmoc-Ala-Gly-OH

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research compound

ApplicationSame Use

Allyl (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-aminobutanoate

CAS688316-86-1

research compound

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L-Valinamide hydrochloride

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N-Formylglycine ethyl ester

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Safety Reference

Harmful
Harmful
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name

(2S)-6-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid

InChIKey

JYEVQYFWINBXJU-QFIPXVFZSA-N

SMILES

CC(C)(C)OC(=O)N[C@@H](CCCCNC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)C(=O)O

Synonyms (17)
  • Boc-L-Lys(Fmoc)-OH
  • Boc-Lys(Fmoc)-OH
  • BocLys(Fmoc)
  • N-Boc-N'-Fmoc-L-Lysine
  • N2-Boc-N6-Fmoc-L-lysine