16939-13-2

Basic information

• Product Name: 3,4-diphenylthiophene
• Synonyms: 3,4-Diphenylthiophene; thiophene, 3,4-diphenyl-
• CAS NO: 16939-13-2
• Molecular Formula: C₁₆H₁₂S
• Molecular Weight: 236.3315
• Mol File: 16939-13-2.mol
• Article Data: 30

Chemical Properties

• Boiling Point: 289.1°C at 760 mmHg
• Flash Point: 94.2°C
• Density: 1.128g/cm³
• Vapor Pressure: 0.0039mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: 3,4-diphenylthiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-diphenylthiophene(16939-13-2)
• EPA Substance Registry System: 3,4-diphenylthiophene(16939-13-2)

Safety Data

• Hazardous Substances Data: 16939-13-2(Hazardous Substances Data)

Upstream product

• 19799-42-9 3,4-bis(phenyl)thiophene-2,5-dicarboxylic acid 
• 3141-26-2 3,4-dibromothiophene 
• 108-86-1 bromobenzene 
• 2461-80-5 diphenacyl sulfide 
• 2548-47-2 2,3-diphenyl-1,3-butadiene 
• 116195-00-7 9,10-dihydro-9,10-(1,3-epidithio-2-methano-2-p-methoxyphenyl-1-oxide)-propanoanthracene 
• 4661-46-5 2-carboxybenzene diazonium chloride 
• 100989-94-4 3-(2-chlorophenyl)-4-phenylthiophene 
• 76390-38-0 3,6-Dihydro-2,2,4,5-tetraphenyl-2H-thiopyran 
• 100990-20-3 cis-3,4-dihydroxy-3,4-diphenylthiolane 
• 92802-27-2 2,6-diphenyl-1,4-dithiine 
• 536-74-3 phenylacetylene 
• 70-11-1 α-bromoacetophenone 
• 1826-12-6 4-phenyl-thiazole 

Downstream Products

• 54119-53-8 3,4-diphenylthiopnene 1,1-dioxide 
• 83125-18-2 2,5-dibromo-3,4-diphenylthiophene 
• 609369-02-0 2,5-bis(hydroxymethylphenyl)-3,4-diphenylthiophene 
• 181218-41-7 3,4-diphenyl-2,5-bis(chloromethyl)thiophene 
• 885484-67-3 9-(3,4-diphenylthiophen-2-yl)-fluoren-9-ol 
• 885484-68-4 3-phenyl-spiro[[8H]indeno[2,1-b]thiophene-8,9'-fluorene] 
• 885484-70-8 2-(9-hydroxy-fluoren-9-yl)-3-phenyl-spiro[[8H]indeno[2,1-b]thiophene-8,9'-fluorene] 
• 836606-04-3 3,4-diphenylthiophene-2,5-diylbis(methylene-N,N-diethyldithiocarbamate) 
• 6363-19-5 2,3-diphenylanthracene-9,10-dione 
• 249512-73-0 6,7-diphenyl-[1,4]naphthoquinone 
• 682774-05-6 2,3,6,7-tetraphenyl-9,10-anthraquinone 
• 42925-40-6 cis-3,4-diphenyl-tetrahydro-thiophene-1,1-dioxide 
• 69888-51-3 3,4-diphenyl-3-sulfolene 
• 403504-13-2 2-(6-(2-pyridyl)-2-pyridyl)-3,4-diphenylthiophene 

Relevant articles and documents

Diselenide-assisted sulfuration of dienes

Various diselenides assist in the sulfuration of dienes giving cyclic di- and tetrasulfides as main products. The reaction requires a 2-fold excess of diselenides to be efficient. Catalytic amounts of diselenides result in lower yields. This is likely due to secondary reactions (polymerization, aromatization) occurring during extended reaction times under catalytic conditions. It was verified that the sulfur-transferring properties of diselenatetrasulfides are virtually identical to those of diselenides combined with sulfur. Contrary to previous claims, not only the cyclic diselenatetrasulfide but also linear diselenatetrasulfides (RSeSnSeR) transfer sulfur to dienes. A mechanism is proposed and its implications to the nature of diatomic sulfur are discussed.

Accessing π-expanded heterocyclics beyond dibenzothiophene: Syntheses and properties of phenanthrothiophenes

A series of phenanthrothiophenes are designed and synthesized from polyarylthiophenes through regioselective Scholl reactions in one step using iron chloride as catalyst. The molecular structures of these heteroarenes displayed multiple twisted fjords, which perturb the shapes of the polycyclic frameworks to pack in slipped to near-perfect face-to-face styles in parallel or antiparallel packings. Field-effect transistor devices using single crystals of 6,12-difluorodiphenanthro[9, 10-b:9′, 10′]thiophene gave a hole mobility of 0.22 cm2 V?1 s?1.

H-type acceptor material and preparation method thereof

The invention discloses an H-type acceptor material and a preparation thereof, and belongs to the field of organic photoelectric material preparation. The acceptor material cannot rotate as both two arms of the acceptor material are connected with a core