1380787-18-7

Basic information

• Product Name: 3-(7-(4-(bis(4-(hexyloxy)phenyl)amino)phenyl)-2,3-dihydrothieno[3,4-b]-[1,4]dioxin-5-yl)benzo[c]thiophene-1-carbaldehyde
• CAS NO: 1380787-18-7
• Molecular Weight: 746.004
• Mol File: 1380787-18-7.mol

Chemical Properties

• CAS DataBase Reference: 3-(7-(4-(bis(4-(hexyloxy)phenyl)amino)phenyl)-2,3-dihydrothieno[3,4-b]-[1,4]dioxin-5-yl)benzo[c]thiophene-1-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(7-(4-(bis(4-(hexyloxy)phenyl)amino)phenyl)-2,3-dihydrothieno[3,4-b]-[1,4]dioxin-5-yl)benzo[c]thiophene-1-carbaldehyde(1380787-18-7)
• EPA Substance Registry System: 3-(7-(4-(bis(4-(hexyloxy)phenyl)amino)phenyl)-2,3-dihydrothieno[3,4-b]-[1,4]dioxin-5-yl)benzo[c]thiophene-1-carbaldehyde(1380787-18-7)

Safety Data

• Hazardous Substances Data: 1380787-18-7(Hazardous Substances Data)

Upstream product

• 1380787-17-6 3-(7-(4-(bis(4-(hexyloxy)phenyl)amino)phenyl)-2,3-dihydrothieno[3,4-b]-[1,4]dioxin-5-yl)-4,7-dihydro-4,7-dihydro-4,7-ethanobenzo[c]thiophene-1-carbaldehyde 
• 1159894-39-9 4-(7-bromo-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-N,N-bis(4-(hexyloxy)phenyl)aniline 
• 1159894-38-8 2-[4-[N,N-bis-(4-hexyloxyphenyl)amino]phenyl]-3,4-(ethylenedioxy)thiophene 

Downstream Products

• 1380786-89-9 C₄₈H₄₈N₂O₆S₂ 

Relevant articles and documents

Tuning the spectroscopic, electrochemical, and photovoltaic properties of triaryl amine based sensitizers through ring-fused thiophene bridges

The ring-fused thiophene derivatives benzo[c]thiophene and its precursor bicyclo[2.2.2]octadiene (BCOD) have been introduced as π-conjugated spacers for organic push-pull sensitizers with dihexyloxy-substituted triphenylamine as donor and cyanoacrylic acid as acceptor (OL1-OL6). The effects of the fused ring on the spectroscopic and electrochemical properties of these sensitizers and their photovoltaic performance in dye-sensitized solar cells have been evaluated. Introduction of a binary benzo[c]thiophene and ethylenedioxy thiophene as π bridge caused a significant red shift of the characteristic intramolecular charge-transfer band to 642 nm. It is found that the sensitizer OL3, which contains one benzo[c]thiophene unit as π linker, gives the highest overall conversion efficiency of 5.03% among all these dyes. Copyright