C21H23NO4
353.4 g/mol
Research ReagentWarning
(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid
CAS77284-32-3EC692-798-8
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound
This compound is an Fmoc-protected derivative of L-norleucine, a building block used in solid-phase peptide synthesis. Its significance lies in its role as a research reagent for incorporating norleucine residues into synthetic 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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CAS 77284-32-3
Related Compounds
StrongStructure SimilarSimilarity 0.86
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Safety Reference
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
Identifiers
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
InChIKey
VCFCFPNRQDANPN-IBGZPJMESA-N
SMILES
CCCC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
Synonyms (16)
- Fmoc-Ahx-OH
- Fmoc-L-2-aminohexanoic acid
- Fmoc-L-Nle-OH
- Fmoc-L-norleucine
- Fmoc-L-norleucine Fmoc-Nle-OH
- Fmoc-Nle
- Fmoc-Nle-OH
- Fmoc-norleucine
- N-Fmoc-L-norleucine