202-72-2

Basic information

• Product Name: DIPHENANTHRO[9,10-B:9',10'-D]THIOPHENE
• Synonyms: DIPHENANTHRO[9,10-B:9',10'-D]THIOPHENE
• CAS NO: 202-72-2
• Molecular Formula: C28H16S
• Molecular Weight: 384.49
• Mol File: 202-72-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 259-260 °C
• Boiling Point: 676.7±24.0 °C(Predicted)
• Appearance: /
• Density: 1.355±0.06 g/cm3(Predicted)
• CAS DataBase Reference: DIPHENANTHRO[9,10-B:9',10'-D]THIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: DIPHENANTHRO[9,10-B:9',10'-D]THIOPHENE(202-72-2)
• EPA Substance Registry System: DIPHENANTHRO[9,10-B:9',10'-D]THIOPHENE(202-72-2)

Safety Data

• Hazardous Substances Data: 202-72-2(Hazardous Substances Data)

Upstream product

• 4688-76-0 2-Biphenylboronic acid 
• 1884-68-0 tetraphenylthiophene 
• 16939-13-2 3,4-diphenylthiophene 
• 583-53-9 2,3-dibromobenzene 
• 3958-03-0 Tetrabromothiophene 
• 5565-85-5 5,5-dimethyl-5H-dibenzo[b,d]stannole 
• 61708-79-0 9-mercaptophenanthrene 
• 61832-78-8 di-[9]phenanthryl sulfide 
• 110129-05-0 bis(9-phenanthryl) disulfide 
• 95033-74-2 rac-10,10'-dihydroxy-9,9'-biphenanthryl 
• 190841-70-4 Dimethyl-thiocarbamic acid O-(10'-dimethylthiocarbamoyloxy-[9,9']biphenanthrenyl-10-yl) ester 
• 124108-63-0 di-[9]phenanthryl sulfoxide 

Relevant articles and documents

A novel compound, a method for preparing the same, and a negative active material for a redox flow battery including the new compound, and a redox flow battery comprising the same

The present invention provides a novel compound having an excellent redox stability and a low reduction potential. The present invention relates to a negative active material for a redox flow battery comprising a novel compound and a novel compound, and a

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.

9-Stannafluorenes: 1,4-dimetal equivalents for aromatic annulation by double cross-coupling

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