606124-56-5

Basic information

• Product Name: ((1R,2R)-1-Benzyl-2-benzyloxy-but-3-ynyl)-(9-phenyl-9H-fluoren-9-yl)-amine
• Synonyms: ((1R,2R)-1-Benzyl-2-benzyloxy-but-3-ynyl)-(9-phenyl-9H-fluoren-9-yl)-amine
• CAS NO: 606124-56-5
• Molecular Weight: 505.659
• Mol File: 606124-56-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((1R,2R)-1-Benzyl-2-benzyloxy-but-3-ynyl)-(9-phenyl-9H-fluoren-9-yl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: ((1R,2R)-1-Benzyl-2-benzyloxy-but-3-ynyl)-(9-phenyl-9H-fluoren-9-yl)-amine(606124-56-5)
• EPA Substance Registry System: ((1R,2R)-1-Benzyl-2-benzyloxy-but-3-ynyl)-(9-phenyl-9H-fluoren-9-yl)-amine(606124-56-5)

Safety Data

• Hazardous Substances Data: 606124-56-5(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 606124-54-3 (3R,4R)-5-Phenyl-4-(9-phenyl-9H-fluoren-9-ylamino)-pent-1-yn-3-ol 

Downstream Products

• 577979-03-4 methyl N-{(2S,3R)-2-O-benzyl-4-phenyl-3-[9-phenyl-9-fluorenyl-amino]-butanoyl}-L-leucine 
• 58970-76-6 bestatin 
• 577978-91-7 (2S,3R)-2-O-benzyl-4-phenyl-3-[(9-phenyl-9-fluorenyl)-amino]-phenylbutanoic acid 

Relevant articles and documents

Diastereoselective synthesis of syn-aminoalcohols via contributing CH-π interaction: Simple synthesis of (-)-bestatin

1H NMR and X-ray crystallography studies revealed that a CH-π and chelation control in aromatic aminoaldehydes (1-6) effects a highly diastereoselective addition to afford optically active syn-aminoalcohols (1a-6a). This methodology was applied to the synthesis of (-)-bestatin.