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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Related Compounds
StrongStructure SimilarSimilarity 0.86
Fmoc-L-Norvaline
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pharmaceutical intermediate
SimilarStructure SimilarSimilarity 0.77
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pharmaceutical intermediate
SimilarStructure SimilarSimilarity 0.77
Nalpha-Fmoc-L-lysine hydrochloride
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pharmaceutical intermediate
SimilarStructure SimilarSimilarity 0.77
N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-lysine hydrochloride
CAS201002-47-3
pharmaceutical intermediate
ApplicationSame Use
Fmoc-L-tert-leucine
CAS132684-60-7
research compound
ApplicationSame Use
N-Fmoc-L-Glutamine
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research compound
ApplicationSame Use
Fmoc-D-proline
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research compound
ApplicationSame Use
Fmoc-N-methyl-D-leucine
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research compound
Related Reading
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
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