C23H26N2O5
410.5 g/mol
Research ReagentWarning
Fmoc-Lys(Ac)-OH
CAS159766-56-0
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound
Fmoc-Lys(Ac)-OH is a protected amino acid derivative used as a building block in solid-phase peptide synthesis. The Fmoc group protects the alpha-amino group, while the acetylated lysine side chain allows for selective incorporation of acetyllysine into peptide sequences.
Building block for peptide synthesisResearch reagent for incorporating acetyllysine into peptides
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 0.86
N,N'-Bis-Fmoc-L-lysine
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research compound
SimilarStructure SimilarSimilarity 0.76
N'-Fmoc-N-Cbz-L-Lysine
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pharmaceutical intermediate
SimilarStructure SimilarSimilarity 0.76
N6-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N2-[(phenylmethoxy)carbonyl]-L-lysine
CAS105751-18-6
pharmaceutical intermediate
SimilarStructure SimilarSimilarity 0.74
N-Fmoc-N'-allyoxycarbonyl-L-lysine
CAS146982-27-6
pharmaceutical intermediate
ApplicationSame Use
(S)-N-Fmoc-4-Bromophenylalanine
CAS198561-04-5
research compound
ApplicationSame Use
(S)-N-Fmoc-3-(2-naphthyl)alanine
CAS112883-43-9
research compound
ApplicationSame Use
Fmoc-N-methyl-L-alloisoleucine
CAS1821797-58-3
research compound
ApplicationSame Use
4-Methylphenyl-L-alanine
CAS1991-87-3
research compound
Related Reading
Safety Reference
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
(2S)-6-acetamido-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
InChIKey
HQLBYVWJOXITAM-NRFANRHFSA-N
SMILES
CC(=O)NCCCC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
Synonyms (10)
- Fmoc-L-Lys(Ac)-OH
- Fmoc-Lys(Ac)
- Fmoc-Lys(Ac)-OH
- Fmoc-N'-Acetyl-L-lysine
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