C23H27NO5
397.5 g/mol
Research ReagentWarning
N-((9H-Fluoren-9-ylmethoxy)carbonyl)-O-isopropyl-L-threonine
CAS71989-35-0EC276-261-1
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound
This compound is an Fmoc-protected amino acid reagent used in solid-phase peptide synthesis. It features a fluorenylmethyloxycarbonyl (Fmoc) protecting group and tert-butyl ether side-chain protection, making it suitable for the stepwise assembly of peptides.
Solid-phase peptide synthesisLaboratory peptide research
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.
Sourcing or supplying this compound?
List your inventory or post a purchase request
CAS 71989-35-0
Related Compounds
SimilarStructure SimilarSimilarity 0.77
(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methoxybutanoic acid
CAS928063-81-4
pharmaceutical intermediate
ApplicationSame Use
Fmoc-D-phenylalanine
CAS86123-10-6
research compound
ApplicationSame Use
N-Fmoc-6-aminohexanoic acid
CAS88574-06-5
research compound
ReferenceSame Category
O-tert-Butyl-L-threonine methyl ester hydrochloride
CAS71989-43-0
research compound
ReferenceSame Category
D-6-Oxopipecolinic acid
CAS72002-30-3
research compound
ReferenceSame Category
DdATP trisodium
CAS72029-21-1
research compound
ReferenceSame Category
6-[5-(2-Oxo-Hexahydro-Thieno[3,4-D]Imidazol-4-Yl)-Pentanoylamino]-Hexanoic Acid
CAS72040-64-3
research compound
Referencestereoisomer of
Fmoc-O-tert-butyl-D-threonine
CAS138797-71-4
pharmaceutical intermediate
Safety Reference
Warning
H400Very toxic to aquatic life
H410Very toxic to aquatic life with long lasting effects
Identifiers
IUPAC Name
2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]butanoic acid
InChIKey
LZOLWEQBVPVDPR-UHFFFAOYSA-N
SMILES
CC(C(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)OC(C)(C)C
Synonyms (8)
- Fmoc-D-Thr(But)-OH
- Fmoc-Thr(But)-OH