Fmoc-D-Asp-OAll

• CAT Number: L033780
• CAS Number: 204246-17-3
• Molecular Formula: C22H21NO6
• Molecular Weight: 395.40
• Purity: ≥95%
• IUPAC Name: (3R)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-prop-2-enoxybutanoic acid
• InChI: InChI=1S/C22H21NO6/c1-2-11-28-21(26)19(12-20(24)25)23-22(27)29-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h2-10,18-19H,1,11-13H2,(H,23,27)(H,24,25)/t19-/m1/s1
• InChIKey: ZJMVIWUCCRKNHY-LJQANCHMSA-N
• SMILES: C=CCOC(=O)[C@@H](CC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Fmoc-D-Asp-OAll（Cat No.:L033780）is a specialized amino acid derivative widely used in peptide synthesis. It features the fluorenylmethyloxycarbonyl (Fmoc) group, which protects the amino functionality during synthesis, allowing for stepwise construction of peptides under mild conditions. The D-aspartic acid (D-Asp) backbone provides a chiral center, essential for the creation of peptides with specific biological activities. The O-allyl (OAll) ester group protects the carboxylic acid, facilitating selective deprotection strategies. This derivative is crucial for researchers developing peptides for therapeutic applications, ensuring precision in peptide chain assembly.