1332882-94-6

Basic information

• Product Name: 4'-({(R)-2,3-bis[di(tert-butoxycarbonylmethyl)amino]propionyl}amino)-1,1'-biphenyl-4-carboxylic acid benzyl ester
• Synonyms: 4'-({(R)-2,3-bis[di(tert-butoxycarbonylmethyl)amino]propionyl}amino)-1,1'-biphenyl-4-carboxylic acid benzyl ester
• CAS NO: 1332882-94-6
• Molecular Weight: 846.031
• Mol File: 1332882-94-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4'-({(R)-2,3-bis[di(tert-butoxycarbonylmethyl)amino]propionyl}amino)-1,1'-biphenyl-4-carboxylic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-({(R)-2,3-bis[di(tert-butoxycarbonylmethyl)amino]propionyl}amino)-1,1'-biphenyl-4-carboxylic acid benzyl ester(1332882-94-6)
• EPA Substance Registry System: 4'-({(R)-2,3-bis[di(tert-butoxycarbonylmethyl)amino]propionyl}amino)-1,1'-biphenyl-4-carboxylic acid benzyl ester(1332882-94-6)

Safety Data

• Hazardous Substances Data: 1332882-94-6(Hazardous Substances Data)

Upstream product

• 99768-12-4 4-methoxycarbonylphenylboronic acid 
• 586-78-7 para-nitrophenyl bromide 
• 5730-75-6 4'-nitro-1,1'-biphenyl-4-carboxylic acid methyl ester 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 860030-06-4 (R)-2,3-bis[di(tert-butoxycarbonylmethyl)amino] propionic acid 
• 137058-70-9 4'-amino-1,1'-biphenyl-4-carboxylic acid benzyl ester 

Relevant articles and documents

Dynamics of the glycosidic bond: Conformational space of lactose

The dynamics of the glycosidic bond of lactose was studied by a paramagnetic tagging-based NMR technique, which allowed the collection of an unusually large series of NMR data for a single compound. By the use of distance- and orientation-dependent residual dipolar couplings and pseudocontact shifts, the simultaneous fitting of the probabilities of computed conformations and the orientation of the magnetic susceptibility tensor of a series of lanthanide complexes of lactose show that its glycosidic bond samples syn/syn, anti/syn and syn/anti φ/I regions of the conformational space in water. The analysis indicates a higher reliability of pseudocontact shift data as compared to residual dipolar couplings with the presently available weakly orienting paramagnetic tagging technique. The method presented herein allows for an improved understanding of the dynamic behaviour of oligosaccharides. Copyright