2-(N-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethyl)-2-(2-(((benzhydryloxy)carbonyl)amino)-6-oxo-5H-purin-9(6H)-yl)acetamido)acetic acid

• CAT Number: L002823
• CAS Number: 186046-83-3
• Molecular Formula: C40H35N7O8
• Molecular Weight: 741.70
• Purity: ≥95%
• IUPAC Name: 2-[[2-[(2E)-2-benzhydryloxycarbonylimino-6-oxo-5H-purin-9-yl]acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethyl]amino]acetic acid
• InChI: InChI=1S/C40H35N7O8/c48-32(46(22-33(49)50)20-19-41-39(52)54-23-31-29-17-9-7-15-27(29)28-16-8-10-18-30(28)31)21-47-24-42-34-36(47)43-38(44-37(34)51)45-40(53)55-35(25-11-3-1-4-12-25)26-13-5-2-6-14-26/h1-18,24,31,35H,19-23H2,(H,41,52)(H,49,50)(H2,43,44,45,51,53)
• InChIKey: ZNHVLNAONKUINW-UHFFFAOYSA-N
• SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)OC(=O)NC3=NC4=C(C(=O)N3)N=CN4CC(=O)N(CCNC(=O)OCC5C6=CC=CC=C6C7=CC=CC=C57)CC(=O)O

2-(N-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethyl)-2-(2-(((benzhydryloxy)carbonyl)amino)-6-oxo-5H-purin-9(6H)-yl)acetamido)acetic acid（Cat No.:L002823）is a highly complex, multifunctional molecule used primarily in peptide and nucleotide chemistry. It features protective groups such as Fmoc and Cbz for amino functionalities, facilitating stepwise synthesis and stability during reaction sequences. The compound incorporates a purine-based structure, often resembling guanine analogs, making it suitable for modified nucleoside synthesis or biologically active conjugates. It plays a role in drug development, particularly in designing enzyme inhibitors or molecular probes. Due to its structural complexity, it requires precise handling and conditions to maintain integrity during chemical reactions.