1309868-11-8

Basic information

• Product Name: 2-(benzofuran-2-yl)-5-phenyloxazole
• Synonyms: 2-(benzofuran-2-yl)-5-phenyloxazole
• CAS NO: 1309868-11-8
• Molecular Weight: 261.28
• Mol File: 1309868-11-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(benzofuran-2-yl)-5-phenyloxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(benzofuran-2-yl)-5-phenyloxazole(1309868-11-8)
• EPA Substance Registry System: 2-(benzofuran-2-yl)-5-phenyloxazole(1309868-11-8)

Safety Data

• Hazardous Substances Data: 1309868-11-8(Hazardous Substances Data)

Upstream product

• 1006-68-4 5-phenyloxazole 
• 91703-34-3 2-(β,β-dibromovinyl)phenol 
• 536-74-3 phenylacetylene 
• 884866-01-7 1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole 
• 4265-16-1 2-formylbenzo[b]furan 
• 1613510-92-1 (E)-N-styrylbenzofuran-2-carboxamide 
• 6783-05-7 trans-2-phenylvinylboronic acid 

Relevant articles and documents

Rh-Catalyzed Formal [3+2] Cyclization for the Synthesis of 5-Aryl-2-(quinolin-2-yl)oxazoles and Its Applications in Metal Ions Probes

A facile and efficient strategy for the synthesis of 5-aryl-2-(quinolin-2-yl)oxazoles via rhodium-catalyzed formal [3+2] cyclization of 4-aryl-1-tosyl-1H-1,2,3-triazoles with quinoline-2-carbaldehydes has been described. The protocol employs mild conditions and offers good yields of diverse 2,5-aryloxazole derivatives with a broad reaction scope. It is amenable to gram-scale synthesis and easily transformation. Moreover, this 5-aryl-2-(quinolin-2-yl)oxazole skeleton is indeed a new fluorophore and its applications in metal ions probes are also investigated and showed fluorescent responses to mercury ion.

One-pot synthesis of benzofused heteroaryl azoles via tandem C-heteroatom coupling/C-H activation of azoles

The Cu(i) or Pd(ii)-catalyzed cross-couplings of gem-dihaloolefins with azoles via tandem C-heteroatom coupling/C-H activation for the preparation of benzofused heteroaryl azoles have been developed.