1384110-11-5

Basic information

• Product Name: 1,4-phenylenebis((3,3'''-didodecyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)methanol)
• Synonyms: 1,4-phenylenebis((3,3'''-didodecyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)methanol)
• CAS NO: 1384110-11-5
• Molecular Weight: 1468.46
• Mol File: 1384110-11-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,4-phenylenebis((3,3'''-didodecyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)methanol)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-phenylenebis((3,3'''-didodecyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)methanol)(1384110-11-5)
• EPA Substance Registry System: 1,4-phenylenebis((3,3'''-didodecyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)methanol)(1384110-11-5)

Safety Data

• Hazardous Substances Data: 1384110-11-5(Hazardous Substances Data)

Upstream product

• 623-27-8 terephthalaldehyde, 
• 162151-09-9 3,3?-didodecyl-2,2′;5′,2″;5″,2?-quaterthiophene 

Downstream Products

• 1384110-06-8 1,4-bis((3,3'''-didodecyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)methyl)benzene 

Relevant articles and documents

Bridged 3,3″′-didodecylquaterthiophene-based dimers: Design, synthesis, and optoelectronic properties

Five functionalized quaterthiophene dimers including a non-conjugated bridge have been designed and efficiently synthesized. The synthetic pathways explored toward these dimers revealed unexpected features, such as the direct formation of secondary and tertiary quaterthiophene amines through a procedure initially developed for the preparation of primary amine exclusively. All these dimers possess a promising potential for the elaboration of semiconducting materials with a charge transport of higher dimensionality compared to quaterthiophene.