360772-76-5

Basic information

• Product Name: N,N'-Bis(benzyloxy)-5-tetradecyl-4,7-dioxasebacic acid diamide
• CAS NO: 360772-76-5
• Molecular Weight: 612.85
• Mol File: 360772-76-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N'-Bis(benzyloxy)-5-tetradecyl-4,7-dioxasebacic acid diamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-Bis(benzyloxy)-5-tetradecyl-4,7-dioxasebacic acid diamide(360772-76-5)
• EPA Substance Registry System: N,N'-Bis(benzyloxy)-5-tetradecyl-4,7-dioxasebacic acid diamide(360772-76-5)

Safety Data

• Hazardous Substances Data: 360772-76-5(Hazardous Substances Data)

Upstream product

• 360772-78-7 5-Tetradecyl-4,7-dioxasebacic acid diethyl ester 
• 151331-30-5 5-tetradecyl-4,7-dioxa-1,9-decadiene 
• 151331-31-6 5-tetradecyl-4,7-dioxa-1,10-decanediol 
• 6920-24-7 hexadecane-1,2-diol 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 

Relevant articles and documents

Synthesis of novel Hg2+ receptors based on N-benzyloxyamide derivatives and their application to anion-selective electrodes

Novel Hg2+ receptors having two N-benzyloxyamide groups are synthesized, and their complexation ability toward metal cations is examined. The structure of the formed complexes was elucidated by ESI-MS and 1H NMR spectroscopy. Deprotonation of the amide groups allows the receptors to form stable complexes with Hg2+. As an application of this neutral Hg2+ complex, an anion-selective electrode combined with a cationic additive is prepared, and exhibits an anti-Hofmeister selectivity pattern with enhanced selectivity for the iodide anion. The overall selectivity pattern of the electrode is I- > ClO4- > SCN- ≈ Br- > salicylate- > NO2- > Cl- > NO3- ? HCO3- > SO42- > F- > H2PO4-.