1123867-50-4

Basic information

• Product Name: 6-phenylnaphtho[1,2-b]benzofuran
• Synonyms: 6-phenylnaphtho[1,2-b]benzofuran
• CAS NO: 1123867-50-4
• Molecular Weight: 294.353
• Mol File: 1123867-50-4.mol

Chemical Properties

• CAS DataBase Reference: 6-phenylnaphtho[1,2-b]benzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenylnaphtho[1,2-b]benzofuran(1123867-50-4)
• EPA Substance Registry System: 6-phenylnaphtho[1,2-b]benzofuran(1123867-50-4)

Safety Data

• Hazardous Substances Data: 1123867-50-4(Hazardous Substances Data)

Upstream product

• 1123867-46-8 2-(2-(2-phenylethynyl)phenyl)-benzofuran 
• 533-58-4 2-Iodophenol 
• 143192-60-3 2-(phenylethynyl)phenylacetylene 
• 30069-72-8 2,3-diphenylnaphthalen-1-ol 
• 3376-24-7 N-tert-butyl-α-phenylnitrone 
• 886-38-4 diphenylcyclopropenone 

Relevant articles and documents

Nitrone Directing Groups in Rhodium(III)-Catalyzed C?H Activation of Arenes: 1,3-Dipoles versus Traceless Directing Groups

Functionalizable directing groups (DGs) are highly desirable in C?H activation chemistry. The nitrone DGs are explored in rhodium(III)-catalyzed C?H activation of arenes and couplings with cyclopropenones. N-tert-butyl nitrones bearing a small ortho subst

Polyaromatic ribbon/benzofuran fusion via consecutive endo cyclizations of enediynes

The Sonogashira/5-endo-dig/6-endo-dig cascade fuses a polycyclic aromatic backbone to the electron-rich furan subunit. The transformation proceeds in modest yields as a one-pot reaction. Efficiency of the full cascade is increased by removal of base prior

Halopalladation/decarboxylation/carbon-carbon forming domino process: synthesis of 5-halo-6-substituted benzo[b]naphtho[2,1-d]furans

A novel and general halopalladation/decarboxylation/carbon-carbon forming domino protocol is described for the synthesis of 5-halo-6-substituted benzo[b]naphtho[2,1-d]furans. The protocol represents the first example of trapping the σ-vinylpalladium inter