497968-91-9

Upstream product

• 90-04-0 2-methoxy-phenylamine 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 497968-90-8 7-(2-methoxy-4-nitrophenyl)-16-(2-methoxyphenyl)-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane 
• 497969-02-5 3-methoxy-4-[16-(2-methoxyphenyl)-1,4,10,13-tetraoxa-7,16-diazacyclooctadecan-7-yl]phenylamine 
• 497968-94-2 7,16-bis(2-methoxyphenyl)-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane-6,17-dione 
• 497969-01-4 3-methoxy-4-[13-(2-methoxyphenyl)-1,4,10-trioxa-7,13-diazacyclopentadecan-7-yl]phenylamine 
• 497968-89-5 7-(2-methoxy-4-nitrophenyl)-13-(2-methoxyphenyl)-1,4,10-trioxa-7,13-diazacyclopentadecane 
• 182926-58-5 7,13-bis(2-methoxyphenyl)-1,4,10-trioxa-7,13-diazacyclopentadecane 
• 497968-93-1 7,13-bis(2-methoxyphenyl)-1,4,10-trioxa-7,13-diazacyclopentadecane-8,12-dione 
• 155581-87-6 7,16-bis(2-methoxyphenyl)-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane 
• 497968-92-0 1,10-bis(2-methoxyphenyl)-4,7-dioxa-1,10-diazadecane 

Relevant academic research and scientific papers

A red-emissive two-photon fluorescent probe for mitochondrial sodium ions in live tissue

A cyclocyanine (CC)-based organic small molecule two-photon (TP) fluorescent probe (CCNa1) was developed for mitochondrial sodium ion sensing.CCNa1exhibits a low solvatochromic shift and strong TP fluorescence enhancement at 575 nm upon binding to Na

Synthesis of functionalised macrocyclic compounds as Na+ and K+ receptors: A mild and high yielding nitration in water of mono and bis 2-methoxyaniline functionalised crown ethers

The syntheses of the bis-aromatic 15-crown-5 and 18-crown-6-ether derivatives 1 and 2, for the selective recognition of intra- and extracellular concentrations of Na+ and K+, from o-anisidine are described. These compounds were made

Fluorescent switches with high selectivity towards sodium ions: Correlation of ion-induced conformation switching with fluorescence function

Diazacoronand 2 undergoes drastic conformational switching upon binding sodium ions as demonstrated by solution- and solid-state studies, which permit the design of efficient fluorescent PET (photoinduced electron transfer) switches 3a,b.