38135-18-1

Basic information

• Product Name: phenyl-9 indeno(1,2,3 f-g)naphtacene
• Synonyms: phenyl-9 indeno(1,2,3 f-g)naphtacene
• CAS NO: 38135-18-1
• Molecular Weight: 378.473
• Mol File: 38135-18-1.mol

Chemical Properties

• CAS DataBase Reference: phenyl-9 indeno(1,2,3 f-g)naphtacene(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl-9 indeno(1,2,3 f-g)naphtacene(38135-18-1)
• EPA Substance Registry System: phenyl-9 indeno(1,2,3 f-g)naphtacene(38135-18-1)

Safety Data

• Hazardous Substances Data: 38135-18-1(Hazardous Substances Data)

Upstream product

• 40577-78-4 5,11-dibromonaphthacene 
• 38135-10-3 diphenyl-5,11 naphtacene 
• 92-24-0 Tetracen 
• 71-43-2 benzene 
• 59840-55-0 5,11-dichloro-6,12-diphenyl-naphthacene 
• 35058-43-6 6-chloro-5,12-naphthacenequinone 
• 108-86-1 bromobenzene 
• 112175-44-7 phenyl-7 benzoyl-6 benzo(c)fluorene-7H 
• 96416-43-2 5-chloro-6,11-diphenyltetracene 
• 96416-44-3 6-chloro-5,11-diphenyl-naphthacene 
• 27130-32-1 6,11-diphenylnaphthacene 

Relevant articles and documents

Benzo- And Thieno-Annulated Tetracenes: A One-Pot Synthesis via Cross-Dehydrogenative Annulation

A facile method for the direct cross-annulation of unfunctionalized tetracene is reported. The one-pot oxidative cross-dehydrogenative coupling (CDC) between tetracene and aromatic compounds, such as benzene or 2-methylthiophene, furnished annulated products with an extended π-network. Moreover, relative to the benzo-annulated tetracenes, thieno-annulated tetracenes exhibited notably improved photooxidative stability. This behavior stands in sharp contrast with that of tetracene and its derivatives, such as rubrene, which readily engage in photoinduced oxidation reactions.

Domino Cross-Scholl Reaction of Tetracene with Molecular Benzene: Synthesis, Structure, and Mechanism

A domino-type multiple C-H functionalization of tetracene with molecular benzene is reported. Under the typical conditions of the Scholl reaction, a domino reaction occurs between tetracene and six molecules of benzene in one pot to furnish an aromatic compound with a curved π-system. This reaction sequence involves oxidative cross-dehydrogenative coupling/annulation and Friedel-Crafts-type reactions. Eight C-C bonds are formed via this intermolecular domino reaction without mediation by a metal or the assistance of a specific substituent.

Electron-Deficient Tetrabenzo-Fused Pyracylene and Conversions into Curved and Planar π-Systems Having Distinct Emission Behaviors

Polycyclic aromatic compounds containing fully unsaturated five-membered ring(s) have been intensively studied because of their unique properties, which include high electron affinity and reactivity. Reported herein is an efficient route for the synthesis

Isomerisations et cyclisations de derives bifonctionnels des diphenyl-1,4 butadienes Z,Z et E,E. Acces a une cetone derivee du Benzo(c) 7H-fluorene

Furannic diols 1a, 1b, furofurans 2a, 2b and stereoisomers (Z,Z) 4 and (E,E) 5a of 2,3 bis phenyl methylene-1,4 diphenyl butanedione give, with strong acids, the -7H benzo(c) fluorenic ketone, 3.The structure of the compound 3 is demonstrated by bidimensi