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

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• 110129-05-0 bis(9-phenanthryl) disulfide 
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• 124108-63-0 di-[9]phenanthryl sulfoxide 

Relevant articles and documents

Steering Scholl Oxidative Heterocoupling by Tuning Topology and Electronics for Building Thiananographenes and Their Functional N?/C?Congeners

While intramolecular Scholl oxidative coupling between two arenes is common, successful C?C heterocoupling between thiophene and arene is scarce. The latter is due to the notorious reactivity of thiophene towards polymerization under oxidative conditions.

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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