1017260-46-6

Basic information

• Product Name: 5''-(4-(diphenylamino)phenyl)-2,2';5',2''-terthiophen-5-yl-carbaldehyde
• Synonyms: 5''-(4-(diphenylamino)phenyl)-2,2';5',2''-terthiophen-5-yl-carbaldehyde
• CAS NO: 1017260-46-6
• Molecular Weight: 519.712
• Mol File: 1017260-46-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5''-(4-(diphenylamino)phenyl)-2,2';5',2''-terthiophen-5-yl-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5''-(4-(diphenylamino)phenyl)-2,2';5',2''-terthiophen-5-yl-carbaldehyde(1017260-46-6)
• EPA Substance Registry System: 5''-(4-(diphenylamino)phenyl)-2,2';5',2''-terthiophen-5-yl-carbaldehyde(1017260-46-6)

Safety Data

• Hazardous Substances Data: 1017260-46-6(Hazardous Substances Data)

Upstream product

• 267221-88-5 4-(diphenylamino)phenylboronic pinacol ester 
• 735316-11-7 5-iodo-2,2′:5′,2″-terthiophene-5″-carboxaldehyde 
• 94581-95-0 5-bromo-2,2':5',2''-terthiophene 
• 1081-34-1 2,2':5',2''-terthiophene 
• 161726-69-8 5″-bromo-2,2′:5′,2″-terthiophene-5-carboxaldehyde 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 479719-88-5 2-([2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1309674-19-8 2-bromo-5-[4-(N,N-diphenylamino)phenyl]thiophene 
• 201802-67-7 4-(diphenylamino)phenyl boronic acid 
• 7342-41-8 2,2':5',2''-terthiophene-5-carboxaldehyde 
• 3779-27-9 2,2'-bithiophene-5-carboxaldehyde 

Downstream Products

• 1363178-03-3 C₄₆H₄₁N₃O₂S₃ 
• 1429739-58-1 C₄₂H₃₈N₂O₂S₃ 
• 1240407-97-9 C₃₄H₂₂N₂O₂S₃ 

Relevant articles and documents

Synthesis and photoinduced charge stabilization in molecular tetrads featuring covalently linked triphenylamine-oligothiophene-BODIPY-C60

Two covalently linked tetrads comprised of charge stabilizing triphenylamine (TPA)-oligothiophene (bi- or terthiophene, BT or TT) linked at the meso-position of a well-known photosensitizer, BF2-chelated boron dipyrromethene (BODIPY), was furth

Effects of fused thiophene bridges in organic semiconductors for solution-processed small-molecule organic solar cells

Three push-pull organic semiconductors, TPA-Th3-MMN (1), TPA-ThTT-MMN (2), and TPA-ThDTTMMN (3), comprising a triphenylamine donor and a methylene malononitrile acceptor linked by various π-conjugated thiophene units were synthesized, and the effects of the π-conjugated bridging unit on the photovoltaic characteristics of solution-processed small-molecule organic solar cells based on these semiconductors were investigated. Planar bridging units with extended π-conjugation effectively facilitated intermolecular π-π packing interactions in the solid state, resulting in enhanced Jsc values of the SMOSCs fabricated with bulk heterojunction films. Copyright

IMPROVED OLIGOTHIOPHENES

Compounds of Formula (I), wherein T is independently selected from the group consisting of (a). And the variables R1, R2, R3, R4, R5, R6, R7, R8, R9, Ar, L