1416056-57-9

Basic information

• Product Name: 6-fluoro-2,3-bis(3-(octyloxy)phenyl)-5,8-di(thiophen-2-yl)quinoxaline
• Synonyms: 6-fluoro-2,3-bis(3-(octyloxy)phenyl)-5,8-di(thiophen-2-yl)quinoxaline
• CAS NO: 1416056-57-9
• Molecular Weight: 721.016
• Mol File: 1416056-57-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 6-fluoro-2,3-bis(3-(octyloxy)phenyl)-5,8-di(thiophen-2-yl)quinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-fluoro-2,3-bis(3-(octyloxy)phenyl)-5,8-di(thiophen-2-yl)quinoxaline(1416056-57-9)
• EPA Substance Registry System: 6-fluoro-2,3-bis(3-(octyloxy)phenyl)-5,8-di(thiophen-2-yl)quinoxaline(1416056-57-9)

Safety Data

• Hazardous Substances Data: 1416056-57-9(Hazardous Substances Data)

Upstream product

• 367-31-7 4-fluoro-1,2-phenylenediamine 
• 851436-85-6 1-bromo-3-(octyloxy)benzene 
• 1347736-74-6 4,7-dibromo-5-fluoro-benzo[c][1,2,5]thiadiazole 
• 1415800-22-4 5,8-dibromo-6-fluoro-2,3-bis(3-(octyloxy)phenyl)quinoxaline 
• 54663-78-4 tributyl(thien-2-yl)stannane 
• 1100761-32-7 1,2-bis-(3-(octyloxy)phenyl)ethane-1,2-dione 
• 937703-96-3 (3-(octyloxy)phenyl)magnesium bromide 
• 1347736-83-7 3,6-dibromo-4-fluoro-1,2-phenylenediamine 

Downstream Products

• 1416054-08-4 5,8-bis(5-bromothiophen-2-yl)-6-fluoro-2,3-bis(3-(octyloxy)phenyl)quinoxaline 

Relevant articles and documents

Performance comparison of fluorinated and chlorinated donor-acceptor copolymers for polymer solar cells

Fluorinated and chlorinated donor-acceptor alternating copolymers, F-PBTQT and Cl-PBTQT, were synthesized and used as donor materials for polymer solar cells. Among them, Cl-PBTQT exhibited much better device performance, and a single-junction efficiency of 8.16% was achieved, indicating that chlorination could be a better strategy than fluorination to develop highly efficient polymer donors.

Side-Chain Engineering of Benzodithiophene-Fluorinated Quinoxaline Low-Band-Gap Co-polymers for High-Performance Polymer Solar Cells

A new series of donor-acceptor co-polymers based on benzodithiophene and quinoxaline with various side chains have been developed for polymer solar cells. The effect of the degree of branching and dimensionality of the side chains were systematically inve