143029-04-3

Basic information

• Product Name: Ethanamine, 2,2'-oxybis[N-(phenylmethylene)-
• CAS NO: 143029-04-3
• Molecular Formula: C18H20N2O
• Molecular Weight: 280.37
• Mol File: 143029-04-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanamine, 2,2'-oxybis[N-(phenylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanamine, 2,2'-oxybis[N-(phenylmethylene)-(143029-04-3)
• EPA Substance Registry System: Ethanamine, 2,2'-oxybis[N-(phenylmethylene)-(143029-04-3)

Safety Data

• Hazardous Substances Data: 143029-04-3(Hazardous Substances Data)

Upstream product

• 2752-17-2 2,2'-diaminodiethyl ether 
• 100-52-7 benzaldehyde 

Downstream Products

• 64994-17-8 (5R,6R)-5,6-Diphenyl-[1,4,7]oxadiazonane 
• 100-52-7 benzaldehyde 
• 143029-05-4 [1-Phenyl-meth-(E)-ylidene]-{2-[2-(2-{[1-phenyl-meth-(E)-ylidene]-amino}-ethoxy)-ethoxy]-ethyl}-amine 
• 143029-06-5 [1-Phenyl-meth-(E)-ylidene]-(2-{2-[2-(2-{[1-phenyl-meth-(E)-ylidene]-amino}-ethoxy)-ethoxy]-ethoxy}-ethyl)-amine 
• 66582-25-0 1,7-dibenzyl-4-oxa-1,7-diazaheptane 

Relevant articles and documents

Novel synthesis of 1,4-diazacrown ethers by reductive coupling of aromatic diimines

The electroreduction or chemical reduction with zinc powder has been found to be effective to intramolecular coupling of aromatic diimines yielding 1,4-diazacrown ethers. The latter reduction was particularly effective to formation of 1,4-diaza-12-crown-4

MACROHETEROCYCLES. XVI. SYNTHESIS OF MACROCYCLIC LACTONOLACTAMS AND THEIR ION-SELECTIVE CHARACTERISTICS

Sewenteen new macrocyclic lactonolactams were obtained by the acylation of N,N'-dimethylpolyoxyalkanediamines with acid dichlorides in benzene under conditions of high dilution.The coefficients of cationic selectivity in the series of alkali and alkaline-earth metals were determined for them, and compounds which exhibit high calcium selectivity were found.