92060-44-1

Basic information

• Product Name: 6-phenyl-quinoxaline
• Synonyms: 6-phenyl-quinoxaline
• CAS NO: 92060-44-1
• Molecular Weight: 206.247
• Mol File: 92060-44-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 6-phenyl-quinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenyl-quinoxaline(92060-44-1)
• EPA Substance Registry System: 6-phenyl-quinoxaline(92060-44-1)

Safety Data

• Hazardous Substances Data: 92060-44-1(Hazardous Substances Data)

Upstream product

• 4085-18-1 4-amino-3-nitrobiphenyl 
• 122349-88-6 glyoxal bisulfite 
• 91-19-0 2,3-diethynylquinoxaline 
• 938-81-8 N-nitrosoacetanilide 
• 36966-84-4 benzenediazohydroxide 
• 94-36-0 dibenzoyl peroxide 
• 50998-17-9 6-bromoquinoxaline 
• 71-43-2 benzene 
• 201230-82-2 carbon monoxide 
• 98-80-6 phenylboronic acid 
• 107427-52-1 α,α,α',α'-tetrabromo-2,3-dimethyl-pyrazine 
• 536-74-3 phenylacetylene 
• 5153-67-3 nitrostyrene 
• 4458-39-3 biphenyl-3,4-diamine 

Relevant articles and documents

Microwave-enhanced reactivity of non-activated dienophiles towards pyrazine o-quinodimethanes

Microwave irradiation in solvent-free conditions induces cycloaddition reactions of pyrazine o-quinodimethane intermediates with electron-rich dienophiles within 10-15 min to afford quinoxaline derivatives in acceptable yields.

A general synthesis of diarylketones by means of a three-component cross-coupling of aryl and heteroaryl bromides, carbon monoxide, and boronic acids

Pd(OAc)2/di-1-adamantyl-n-butylphosphine (cataCXium A) is highly active in the three-component Suzuki carbonylation and represents the most general catalyst system reported up to now. A broad range of aryl/heteroaryl bromides and aryl boronic acids can be coupled to the corresponding diarylketones at low catalyst loadings.