Fmoc-(S)-3-amino-4-hydroxybutanoic acid t-butyl ester

• CAT Number: L007270
• CAS Number: 1820583-73-0
• Molecular Formula: C23H27NO5
• Molecular Weight: 397.5
• Purity: ≥95%
• IUPAC Name: (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-[(2-methylpropan-2-yl)oxy]butanoic acid
• InChI: InChI=1S/C23H27NO5/c1-23(2,3)29-13-15(12-21(25)26)24-22(27)28-14-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,15,20H,12-14H2,1-3H3,(H,24,27)(H,25,26)/t15-/m0/s1
• InChIKey: SKYFRYZPXHNPOK-HNNXBMFYSA-N
• SMILES: CC(C)(C)OCC(CC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Fmoc-(S)-3-amino-4-hydroxybutanoic acid t-butyl ester（Cat No.:L007270）, is a vital compound in the field of peptide chemistry. This compound belongs to the class of Fmoc (9-fluorenylmethyloxycarbonyl) protected amino acids, frequently utilized in solid-phase peptide synthesis (SPPS). As a building block, it enables the incorporation of specific sequences into peptides, proteins, and peptidomimetics. Researchers use it to design and construct biologically active peptides, serving as a tool in drug discovery, biochemical research, and the development of therapeutic agents. The tert-butyl ester group enhances stability, making it suitable for various peptide synthesis strategies.