15486-07-4

Basic information

• Product Name: 2-<7-(1-ethyl-2-quinolinylidene)-1,3,5-heptatrien-1-yl>-1-ethylquinolinium iodide
• CAS NO: 15486-07-4
• Molecular Weight: 532.467
• Mol File: 15486-07-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-<7-(1-ethyl-2-quinolinylidene)-1,3,5-heptatrien-1-yl>-1-ethylquinolinium iodide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-<7-(1-ethyl-2-quinolinylidene)-1,3,5-heptatrien-1-yl>-1-ethylquinolinium iodide(15486-07-4)
• EPA Substance Registry System: 2-<7-(1-ethyl-2-quinolinylidene)-1,3,5-heptatrien-1-yl>-1-ethylquinolinium iodide(15486-07-4)

Safety Data

• Hazardous Substances Data: 15486-07-4(Hazardous Substances Data)

Upstream product

• 606-55-3 1-ethyl-2-methylquinolinium iodide 
• 82670-38-0 glutaconaldehyde tetraethyl acetal 
• 5608-83-3 5-anilino-penta-2,4-dienal-phenylimine 

Relevant articles and documents

CHEMISTRY OF ENOL ETHERS. LXXIX. REACTION OF GLUTACONALDEHYDE ACETALS AND THEIR DERIVATIVES WITH HETEROCYCLIC COMPOUNDS. THE SYNTHESIS OF TRICARBOCYANINE DYES

The acetal forms of glutaconaldehyde (2,6-dialkoxypyrans, 1,1,5,5-tetralkoxy-2-pentenes, 5,5-dialkoxy-2-pentenals, and 1,3,5,5-tetraalkoxy-1-pentenes) are capable of reacting with the quaternary salts of heterocyclic bases containing an active methyl group in acetic anhydride solution and in the presence of triethylamine with the formation of tricarbocyanine dyes.Syntheses are reported of unsubstituted thio-, indo-, and quinotricarbocyanines and derivatives with various substituents in the polymethine chain.