Fmoc-Asp-NH2

• CAT Number: I016877
• CAS Number: 200335-40-6
• Molecular Formula: C₁₉H₁₈N₂O₅
• Molecular Weight: 354.36
• Purity: ≥95%
• Target: ADC Linker
• Storage: 2-8°C
• IUPAC Name: (3S)-4-amino-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxobutanoic acid
• InChI: InChI=1S/C19H18N2O5/c20-18(24)16(9-17(22)23)21-19(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H2,20,24)(H,21,25)(H,22,23)/t16-/m0/s1
• InChIKey: VHRMWRHTRSQVJJ-INIZCTEOSA-N
• SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC(=O)O)C(=O)N

Fmoc-Asp-NH2（Cat No.:I016877）, is a derivative of aspartic acid commonly used in peptide synthesis. It features the Fmoc (9-fluorenyl methoxycarbonyl) protecting group, which safeguards the amino group during peptide assembly. Fmoc-Asp-NH2 offers stability and compatibility with solid-phase peptide synthesis methods. It serves as a crucial building block for the construction of peptides and peptide analogs in various research and pharmaceutical applications. This compound enables the development of peptide-based therapeutics and aids in drug discovery efforts, making it an important tool in the field of peptide chemistry.