22366-98-9

Usage

Chemical Properties

CLEAR SLIGHTLY YELLOW LIQUID

Upstream product

• 929-59-9 3,6-dioxa-1,8-diaminooctane 
• 31255-10-4 1,2-bis-(2-bromo-ethoxy)-ethane 
• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 
• 143029-05-4 [1-Phenyl-meth-(E)-ylidene]-{2-[2-(2-{[1-phenyl-meth-(E)-ylidene]-amino}-ethoxy)-ethoxy]-ethyl}-amine 
• 58929-79-6 Benzyl-(2-{2-[2-(benzyl-methyl-amino)-ethoxy]-ethoxy}-ethyl)-methyl-amine 
• 112-26-5 1,2-bis(2-chloroethoxy)ethane 
• 74-89-5 methylamine 

Downstream Products

• 181588-22-7 1,10-bis(5-chloro-2-hydroxybenzyl)-1,10-dimethyl-4,7-dioxa-1,10-diazadecane 
• 234753-36-7 (S,S)-2,5,8,17-tetramethyl-3,4-diphenyl-2,5,8,17-tetraaza-11,14-dioxacyclooctadecane-1,6-dione 
• 945384-68-9 C₅₉H₇₃N₃O₁₈ 
• 945384-53-2 C₂₇H₃₇N₉O₇ 

Relevant academic research and scientific papers

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.

Ditertiary diamine compounds

The preparation of ditertiary aliphatic diamines 3 designed as drugs protecting CNS acetylcholinesterase against organophosphate inhibition, is described. Owing to the radicals at the basic nitrogen atoms, these compounds should exist in appreciable amounts both as base and as diammonium ion at biological pH's.