1304773-87-2

Basic information

• Product Name: 2,3-difluoro-1,4-di(2-thienyl)-5,6-diamino-benzene
• Synonyms: 2,3-difluoro-1,4-di(2-thienyl)-5,6-diamino-benzene
• CAS NO: 1304773-87-2
• Molecular Weight: 308.376
• Mol File: 1304773-87-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,3-difluoro-1,4-di(2-thienyl)-5,6-diamino-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-difluoro-1,4-di(2-thienyl)-5,6-diamino-benzene(1304773-87-2)
• EPA Substance Registry System: 2,3-difluoro-1,4-di(2-thienyl)-5,6-diamino-benzene(1304773-87-2)

Safety Data

• Hazardous Substances Data: 1304773-87-2(Hazardous Substances Data)

Upstream product

• 1293389-28-2 5,6‐difluoro‐2,1,3‐benzothiadiazole 
• 1304773-88-3 5,6-difluoro-4,7-di(thiophen-2-yl)benzo[c][1, 2, 5]thiadiazole 
• 1304773-86-1 2,3-difluoro-1,4-di(2-thienyl)-5,6-dinitro-benzene 
• 1283598-32-2 1,4-dibromo-2,3-difluoro-5,6-dinitrobenzene 
• 156682-52-9 1,4-dibromo-2,3-difluoro-benzene 

Downstream Products

• 1596358-45-0 5,8-bis(5-bromothiophen-2-yl)-6,7-difluoro-2,3-diphenylquinoxaline 
• 1596358-51-8 6,7-difluoro-2,3-diphenyl-5,8-di(thiophene-2-yl)quinoxaline 

Relevant articles and documents

Enhanced open-circuit voltages of trifluoromethylated quinoxaline-based polymer solar cells

Three quinoxaline-based conjugated polymers with donor-π-acceptor configurations have been synthesized by Stille coupling reaction. The electron-donating 2,3-dioctylthienyl- substituted benzodithiophene (BDT) unit was linked to the electron-accepting 2,3-

Step-by-step improvement in photovoltaic properties of fluorinated quinoxaline-based low-band-gap polymers

A series of fluorinated quinoxaline-based polymers with typical donor-π-acceptor configurations has been synthesized by Stille coupling reaction. The electron-donating dialkoxy-substituted benzodithiophene (BDT) is connected to the electron-withdrawing 2,