217655-10-2

Basic information

• Product Name: Benzaldehyde, 4-[bis(2-hexyloctyl)amino]-
• CAS NO: 217655-10-2
• Molecular Formula: C35H63NO
• Molecular Weight: 513.891
• Mol File: 217655-10-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 4-[bis(2-hexyloctyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-[bis(2-hexyloctyl)amino]-(217655-10-2)
• EPA Substance Registry System: Benzaldehyde, 4-[bis(2-hexyloctyl)amino]-(217655-10-2)

Safety Data

• Hazardous Substances Data: 217655-10-2(Hazardous Substances Data)

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 115007-16-4 7-(bromomethyl)tridecane 
• 19780-79-1 2-hexyl-1-octanol 

Downstream Products

• 217655-15-7 {4-[(E)-2-(3,5-Dimethoxy-phenyl)-vinyl]-phenyl}-bis-(2-hexyl-octyl)-amine 
• 532948-22-4 4-((E)-2-{4-[bis(2-hexyloctyl)amino]phenyl}ethenyl)benzaldehyde 
• 1161841-97-9 all-(E)-tris[4-(2-{4-[bis(2-hexyloctyl)amino]phenyl}vinyl)phenyl]methanol 
• 217655-17-9 5-((E)-2-{4-[Bis-(2-hexyl-octyl)-amino]-phenyl}-vinyl)-benzene-1,3-diol 
• 532948-32-6 4-((E)-2-{4-[(E)-2-(4-{(E)-2-[4-((E)-2-{4-[bis(2-hexyloctyl)amino]phenyl}ethenyl)phenyl]ethenyl}phenyl)ethenyl]phenyl}ethenyl)benzaldehyde 
• 532948-29-1 4-[(E)-2-(4-{(E)-2-[4-((E)-2-{4-[bis(2-hexyloctyl)amino]phenyl}ethenyl)phenyl]ethenyl}phenyl)ethenyl]benzaldehyde 
• 532948-26-8 4-{(E)-2-[4-((E)-2-{4-[bis(2-hexyloctyl)amino]phenyl}ethenyl)phenyl]ethenyl}benzaldehyde 

Relevant articles and documents

Extension of Conjugation Leading to Bathochromic or Hypsochromic Effects in OPV Series

Four OPV series 1-4 (a-d) with a terminal dialkylamino group as electron donor were prepared by Wittig-Horner reactions. To study the influence of the push-pull effect on the long-wavelength absorption, three of the four series contained terminal acceptor

Extended conjugation in stilbenylsquaraines

Unsymmetrical 1-aryl-3-stilbenylsquaraines 2a-e and 1,3-bis(stilbenyl)squaraines 3a-c were prepared by CC coupling reactions of the corresponding substituted arenes with derivatives of squaric acid (Schemes 2 and 3). Dialkylamino and alkoxy groups enhance the solubility of these dyes and enlarge the intramolecular charge transfer of these donor-acceptor-donor systems. The extended conjugation of the stilbene units - in comparison with arene building blocks - leads to significant bathochromic shifts in the Vis/NIR absorption spectra.