69976-38-1

Basic information

• Product Name: Benzofuran, 2-(4-fluorophenyl)-
• CAS NO: 69976-38-1
• Molecular Formula: C14H9FO
• Molecular Weight: 212.223
• Mol File: 69976-38-1.mol
• Article Data: 54

Chemical Properties

• CAS DataBase Reference: Benzofuran, 2-(4-fluorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzofuran, 2-(4-fluorophenyl)-(69976-38-1)
• EPA Substance Registry System: Benzofuran, 2-(4-fluorophenyl)-(69976-38-1)

Safety Data

• Hazardous Substances Data: 69976-38-1(Hazardous Substances Data)

Upstream product

• 1198340-31-6 (Z)-1-phenoxy-1-(4-fluorophenyl)-2-chloroethylene 
• 60785-20-8 α,β-dichlorovinyl phenyl ether 
• 1765-93-1 4-fluoroboronic acid 
• 352-34-1 4-fluoro-1-iodobenzene 
• 66003-76-7 Diphenyliodonium triflate 
• 403-42-9 1-(4-fluorophenyl)ethanone 
• 71-43-2 benzene 
• 54008-77-4 2-bromo-1-benzofuran 
• 352-13-6 4-flourophenylmagnesium bromide 
• 613-84-3 2-hydroxy-5-methylbenzaldehyde 
• 90-02-8 salicylaldehyde 
• 89122-67-8 (E)-1-hydroxy-2-(4-fluoro)styrylbenzene 
• 533-58-4 2-Iodophenol 
• 60981-57-9 (benzofuran-2-yl)trimethylsilane 

Downstream Products

• 1224447-48-6 2,3-bis(4-fluorophenyl)benzo[b]furan 
• 1259295-24-3 2,2'-bis(4-fluorophenyl)-3,3'-bibenzofuran 

Relevant articles and documents

Acid-promoted selective synthesis of trifluoromethylselenolated benzofurans with Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate

A Br?nsted acid-promoted trifluoromethylselenolation of benzofurans was disclosed by using Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate as a stable and easily prepared electrophilic trifluoromethylselenolating reagent. A wide range of SeCF3-substituted benzofuran derivatives were obtained in moderate to good yields with excellent regioselectivity. The tandem cyclization/trifluoromethylselenolation procedure of 1-methoxy-2-(arylethynyl)benzenes were also realized by engaging FeCl3 as the catalyst.

Photocatalyzed Transition-Metal-Free Oxidative Cross-Coupling Reactions of Tetraorganoborates**

Readily accessible tetraorganoborate salts undergo selective coupling reactions under blue light irradiation in the presence of catalytic amounts of transition-metal-free acridinium photocatalysts to furnish unsymmetrical biaryls, heterobiaryls and arylated olefins. This represents an interesting conceptual approach to forge C?C bonds between aryl, heteroaryl and alkenyl groups under smooth photochemical conditions. Computational studies were conducted to investigate the mechanism of the transformation.

Preparation method of benzofuran derivative

The invention belongs to the field of organic chemical synthesis, and particularly relates to a preparation method of a benzofuran derivative. According to the specific technical scheme, the preparation method of the benzofuran derivative comprises the fo