762269-61-4

Basic information

• Product Name: 5′-(4-(diphenylamino)phenyl)(2,2′-bithiophene)-5-carboxaldehyde
• Synonyms: 5′-(4-(diphenylamino)phenyl)(2,2′-bithiophene)-5-carboxaldehyde
• CAS NO: 762269-61-4
• Molecular Weight: 437.586
• Mol File: 762269-61-4.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: 5′-(4-(diphenylamino)phenyl)(2,2′-bithiophene)-5-carboxaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5′-(4-(diphenylamino)phenyl)(2,2′-bithiophene)-5-carboxaldehyde(762269-61-4)
• EPA Substance Registry System: 5′-(4-(diphenylamino)phenyl)(2,2′-bithiophene)-5-carboxaldehyde(762269-61-4)

Safety Data

• Hazardous Substances Data: 762269-61-4(Hazardous Substances Data)

Upstream product

• 267221-88-5 4-(diphenylamino)phenylboronic pinacol ester 
• 110046-60-1 5'-bromo-2,2'-bithiophene-5-carboxaldehyde 
• 492-97-7 2,2'-Bithiophene 
• 3141-27-3 2,5-dibromothiophen 
• 201802-67-7 4-(diphenylamino)phenyl boronic acid 
• 4701-17-1 5-bromo-2-thiophencarboxaldehyde 
• 38257-52-2 4-(N,N-diphenylamino)iodobenzene 
• 193978-23-3 2-thiopheneboronic acid pinacol ester 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 54663-78-4 tributyl(thien-2-yl)stannane 
• 3779-27-9 2,2'-bithiophene-5-carboxaldehyde 
• 1040281-83-1 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxaldehyde 
• 1309674-19-8 2-bromo-5-[4-(N,N-diphenylamino)phenyl]thiophene 
• 58268-08-9 2-(2-thienyl)-1,3-dioxolane 

Downstream Products

• 1017260-44-4 (E)-2-cyano-3-(5'-(5''-(p-(diphenylamino)phenyl)thiophen-2''-yl)thiophen-2'-yl)acrylic acid 
• 1346644-02-7 5-((5'-(4-(diphenylamino)phenyl)-2,2'-bithiophen-5-yl)methylene)-1-(2-ethylhexyl)-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine-3-carbonitrile 
• 1346644-12-9 5-((5'-(4-(diphenylamino)phenyl)-[2,2'-bithiophen]-5-yl)methylene)-(6-hydroxyhexyl)-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine-3-carbonitrile 
• 918549-96-9 D5L6 
• 1379771-83-1 C₃₄H₂₈N₂O₂S₂ 
• 1429739-57-0 C₃₈H₃₆N₂O₂S₂ 

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

Investigation into the influence of an acrylic acid acceptor in organic D-π-A sensitizers against phototoxicity

Photodynamic therapy (PDT) is a non-invasive, selective, and cost-effective cancer therapy. We previously reported that thiophene-based organic D-π-A sensitizers consist of an electron-donating (D) moiety, a π-conjugated bridge (π) moiety, and an electron-accepting (A) moiety, and are readily accessible and stable templates for photosensitizers that could be used in PDT. In addition, acrylic acid acceptor-containing photosensitizers exert a high level of phototoxicity. This study was an investigation into 1) the possibility of increasing phototoxicity by introducing another carboxyl group or by replacing a carboxyl group with a pyridinium group, and 2) the importance of an alkene in the acrylic acid acceptor for phototoxicity. A review of the design, synthesis, and evaluation of sensitizers revealed that neither dicarboxylic acid nor pyridinium photosensitizers enhance phototoxicity. An evaluation of a photosensitizer without an alkene in the acrylic acid moiety revealed that the alkene was not indispensable in the pursuit of phototoxicity. The obtained results provided new insight into the design of ideal D-π-A photosensitizers for PDT.

N, N -Diphenylanilino-heterocyclic aldehyde-based chemosensors for UV-vis/NIR and fluorescence Cu(ii) detection

Herein, three N,N-diphenylanilino-heterocyclic aldehyde probes (5, 6 and 7) are synthesized, characterized and their sensing behaviour against metal cations tested. Acetonitrile solutions of the three probes show an intramolecular charge-transfer band in