1639428-87-7

Basic information

• Product Name: C₇₂H₇₈N₆O₈
• Synonyms: C₇₂H₇₈N₆O₈
• CAS NO: 1639428-87-7
• Molecular Weight: 1155.45
• Mol File: 1639428-87-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₇₂H₇₈N₆O₈(CAS DataBase Reference)
• NIST Chemistry Reference: C₇₂H₇₈N₆O₈(1639428-87-7)
• EPA Substance Registry System: C₇₂H₇₈N₆O₈(1639428-87-7)

Safety Data

• Hazardous Substances Data: 1639428-87-7(Hazardous Substances Data)

Upstream product

• 851786-15-7 N,N'-di(2-ethylhexyl)-1,7-dibromoperylene-3,4,9,10-bisdicarboximide 
• 167492-64-0 3-(2-ethylhexyloxy)-6-hydroxyphthalonitrile 

Downstream Products

• 261504-18-1 2,3,9,10,16,17,23,24-octakis(octyloxy)-29H,31H-phthalocyanine 
• 1639428-88-8 C₁₄₄H₁₈₆N₁₂O₁₄Zn 
• 1639428-89-9 C₁₃₄H₁₈₀N₁₀O₁₃Zn 
• 1639428-90-2 C₅₂H₆₆N₂O₆ 
• 1639428-91-3 C₆₂H₇₂N₄O₇ 

Relevant articles and documents

Synthesis and photophysical properties of novel phthalocyanine- perylenediimide-phthalocyanine triad and phthalocyanine-perylenediimide dyads

A series of novel multi-component chromophores, one phthalocyanine- perylenediimide-phthalocyanine triad and two phthalocyanine-perylenediimide dyads, were synthesized by covalent linkage between phthalocyanines and perylene-3,4,9,10-bis(dicarboximide) at the bay position of perylene core in one condensation reaction. The photophysical properties of the dyes were presented with wider light absorption from 300 to 800 nm and discussed by interpretation and correlations with previous dyes. Density functional theory at the B3LYP level with 6-31G(d) was performed for geometry and energy optimization. Furthermore, a substitution and elimination reaction at the perylene bay position by using 1,8-diazabicyclo[5,4,0]undec-7-ene as catalyst was performed and its probable mechanism discussed. the Partner Organisations 2014.