(S)-N-Fmoc-2-(4'-pentenyl)glycine

• CAS: 856412-22-1
• Catalog Number: ACM856412221-1
• Category: Amino Acids
• Molecular Weight: 365.4
• Molecular Formula: C22H23NO4
• Description: Fmoc-Lys(Boc)-OH is a chemical compound that belongs to the amino acid family. It is commonly used in the synthesis of peptides and proteins in various scientific experiments. The Fmoc group is a temporary protective group used to protect the amine group of lysine, while the Boc (tert-butoxycarbonyl) group is used to protect the amine group of the alpha amino acid. Fmoc-Lys(Boc)-OH is an important building block for the synthesis of peptides and proteins.
• Synonyms: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hept-6-enoic acid, Fmoc-Lys(Boc)-OH
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)hept-6-enoic acid
• Canonical SMILES: C=CCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
• InChI: 1S/C22H23NO4/c1-2-3-4-13-20(21(24)25)23-22(26)27-14-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h2,5-12,19-20H,1,3-4,13-14H2,(H,23,26)(H,24,25)/t20-/m0/s1
• InChI Key: LRSIYGFZZWFAAI-FQEVSTJZSA-N
• Boiling Point: 589.7±45.0 ℃at 760 mmHg
• Flash Point: 310.5±28.7 ℃
• Density: 1.3±0.1 g/cm³
• Application: Fmoc-Lys(Boc)-OH is widely used in peptide and protein synthesis. It can be used in the synthesis of various peptides with potential applications in drug discovery, such as antimicrobial peptides and anticancer peptides.
• Exact Mass: 365.16272
• Functional Group: Fmoc
• HS Code: 2924299090
• LogP: 5.3
• PSA: 75.63
• Refractive Index: 1.587
• Storage Temperature: Store at -20℃
• Type: Unusual Amino Acids, Building Blocks for Stapled peptides
• Vapor Pressure: 0.0±1.7 mmHg at 25℃