Fmoc-Trp(Boc)-OH

• CAT Number: R043492
• CAS Number: 143824-78-6
• Molecular Formula: C31H30N2O6
• Molecular Weight: 526.589
• Purity: ≥95%
• Synonyms: 1-[(1,1-Dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-tryptophan;?3-[(2S)-2-Carboxy-2-[[[(9H-fluoren-9-yl)methoxy]carbonyl]amino]ethyl]indole-1-carboxylic Acid tert-Butyl Ester
• Storage: -20°C
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]indol-3-yl]propanoic acid
• InChI: InChI=1S/C31H30N2O6/c1-31(2,3)39-30(37)33-17-19(20-10-8-9-15-27(20)33)16-26(28(34)35)32-29(36)38-18-25-23-13-6-4-11-21(23)22-12-5-7-14-24(22)25/h4-15,17,25-26H,16,18H2,1-3H3,(H,32,36)(H,34,35)/t26-/m0/s1
• InChIKey: ADOHASQZJSJZBT-SANMLTNESA-N
• SMILES: CC(C)(C)OC(=O)N1C=C(C2=CC=CC=C21)CC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35

Fmoc-Trp(Boc)-OH is a protected form of the amino acid tryptophan used in peptide synthesis. The Fmoc (fluorenylmethyloxycarbonyl) group protects the amino end, while the Boc (tert-butyloxycarbonyl) group protects the side chain, allowing for selective deprotection during the synthesis process. This compound is essential for creating specific peptides and proteins in biochemical and pharmaceutical research, facilitating the study of protein functions and interactions.