(S)-3-(tert-Butoxycarbonylamino)-2-[(9H-fluoren-9-ylmethoxy)carbonylamino]propionic Acid TCI B6107

Chemical Identity

Other names: (S)-3-(Boc-amino)-2-(Fmoc-amino)propionic Acid · 3-(tert-Butoxycarbonyl)amino-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine · 3-(Boc-amino)-N-Fmoc-L-alanine · Nbeta-Boc-Nalpha-Fmoc-L-2,3-diaminopropioni
CAS No.: 162558-25-0
PubChem: CID 2756103·SID 468590914
Formula: C23H26N2O6
Molecular weight: 426.47 g/mol
Purity: >97.0%(T)(HPLC)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
SMILES: CC(C)(C)OC(=O)NCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey: PKAUMAVONPSDRW-IBGZPJMESA-N
MDL: MDL00235896

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This compound is a doubly protected amino acid derivative featuring Fmoc and Boc orthogonal protecting groups, widely used as a versatile building block in solid-phase peptide synthesis (SPPS). It enables selective deprotection and stepwise modification of diaminopropionic acid residues in complex peptide chains. Common applications include the development of modified peptides, bioactive peptidomimetics, and molecular probes for biochemical and medicinal chemistry research.