26832-42-8

Basic information

• Product Name: 2,3-diphenyl-6-quinoxalinyl methyl ether
• Synonyms: 2,3-diphenyl-6-quinoxalinyl methyl ether;6-methoxy-2,3-diphenylquinoxaline
• CAS NO: 26832-42-8
• Molecular Formula: C₂₁H₁₆N₂O
• Molecular Weight: 312.36454
• Mol File: 26832-42-8.mol
• Article Data: 28

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3-diphenyl-6-quinoxalinyl methyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-diphenyl-6-quinoxalinyl methyl ether(26832-42-8)
• EPA Substance Registry System: 2,3-diphenyl-6-quinoxalinyl methyl ether(26832-42-8)

Safety Data

• Hazardous Substances Data: 26832-42-8(Hazardous Substances Data)

Upstream product

• 134-81-6 benzil 
• 102-51-2 4-methoxy-1,2-phenylenediamine 
• 5877-59-8 (E)-3-methoxy-N-(phenylmethylene)benzenamine 
• 536-74-3 phenylacetylene 
• 59548-39-9 4-methoxyphenylene-1,2-diamine dihydrochloride 
• 96-96-8 4-methoxy-2-nitroaniline 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 451-40-1 phenyl benzyl ketone 
• 100-52-7 benzaldehyde 
• 536-90-3 m-Anisidine 
• 854918-58-4 3-chloro-7-methoxy-2-(methylthio)quinoxaline 
• 854918-83-5 7-methoxy-2-(methylthio)-3-phenylquinoxaline 
• 100-58-3 phenylmagnesium bromide 
• 142168-81-8 3-methoxy-N-[1-(methylthio)-2-nitroethenyl]benzenamine 

Downstream Products

• 60729-21-7 2,3-diphenylquinoxaline-6-ol 

Relevant articles and documents

An efficient and green procedure for the synthesis of quinoxaline derivatives using 3,5-bis(Trifluoromethyl)phenylammonium triflate (bfpat) organocatalyst

The application of 3,5-bis(trifluoromethyl)phenylammonium triflate (BFPAT) as a conven-ient new organocatalyst for the synthesis of quinoxaline derivatives is described. In the presence of BFPAT, one-pot synthesis of a wide variety of quinoxaline derivati

A green solid acid catalyst 12-tungstophosphoric acid H3[PW12O40] supported on g-C3N4 for synthesis of quinoxalines

A green Keggin-type heteropoly-12-tungstophosphoric acid, (H3[PW12O40].12H2O) supported on graphitic carbon nitride g-C3N4 (HPW/g-C3N4-40), was developed for one-pot s

Synthesis method of quinoxaline heterocyclic derivative

The invention discloses a synthesis method of a quinoxaline heterocyclic derivative. An intermolecular redox reaction and a condensation cyclization reaction are carried out on an o-nitroaniline compound and an o-diol compound under the action of a water-soluble alkali to prepare the quinoxaline heterocyclic derivative in one step. Expensive transition metal catalysts and ligands do not need to beused, the water-soluble alkali is used as an accelerant and can be removed in a water washing manner, so that the product has no transition metal residue, the product is easy to separate, the recovery rate is high, and the method is simple in condition, easy to operate and low in equipment requirement; and the water-soluble alkali is used as the accelerant, so the unique byproduct is water, the atom economy is high, and the method has good research and industrial application prospects.