5834-20-8

Basic information

• Product Name: 3-Phenyldibenzofuran
• Synonyms: 3-Phenyldibenzofuran
• CAS NO: 5834-20-8
• Molecular Formula: C₁₈H₁₂O
• Molecular Weight: 244.29
• Mol File: 5834-20-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Phenyldibenzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Phenyldibenzofuran(5834-20-8)
• EPA Substance Registry System: 3-Phenyldibenzofuran(5834-20-8)

Safety Data

• Hazardous Substances Data: 5834-20-8(Hazardous Substances Data)

Upstream product

• 4731-97-9 2-(1,1'-biphenyl-4-yl)phenol 
• 533-58-4 2-Iodophenol 
• 5122-94-1 4-biphenylboronic acid 
• 1434906-61-2 2-(3-phenylphenoxy)-benzoic acid 
• 580-51-8 [1,1'-biphenyl]-3-ol 
• 118-91-2 ortho-chlorobenzoic acid 
• 1444457-59-3 1-(benzofuran-2-yl)-2-phenylbuta-2,3-dienyl acetate 
• 26608-06-0 3-bromodibenzofuran 
• 98-80-6 phenylboronic acid 

Relevant articles and documents

Novel phenylcarbazole type organic compounds and an organic electroluminescent device comprising the same

An organic compound represented by chemical formula 1 and an organic light emitting device including the same are provided. Chemical Formula 1.

General approach to benzo[b]thiophenes, benzo[b]furans, and dibenzofurans via gold-catalyzed cyclization of 1-heteroarylalka-2,3-dienyl acetates

An efficient and mild route to a series of benzo[b]thiophenes, benzo[b]furans, and dibenzofurans through gold-catalyzed benzannulation of 1-heteroarylalka-2,3-dienyl acetates was developed. Two possible pathways of this reaction involving gold carbene and aryl gold intermediates have been proposed on the basis of mechanistic studies.

Synthesis of dibenzofurans via palladium-catalyzed phenol-directed C-H activation/C-O cyclization

A practical, Pd(0)/Pd(II)-catalyzed reaction was developed for phenol-directed C-H activation/C-O cyclization using air as an oxidant. The turnover-limiting step of the process was found to be C-O reductive elimination instead of C-H activation. This reaction can tolerate a variety of functional groups and is complementary to the previous methods for the synthesis of substituted dibenzofurans.