36305-60-9

Basic information

• Product Name: Quinoxaline, 6-chloro-2,3-diphenyl-
• CAS NO: 36305-60-9
• Molecular Formula: C20H13ClN2
• Molecular Weight: 316.79
• Mol File: 36305-60-9.mol
• Article Data: 96

Chemical Properties

• CAS DataBase Reference: Quinoxaline, 6-chloro-2,3-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Quinoxaline, 6-chloro-2,3-diphenyl-(36305-60-9)
• EPA Substance Registry System: Quinoxaline, 6-chloro-2,3-diphenyl-(36305-60-9)

Safety Data

• Hazardous Substances Data: 36305-60-9(Hazardous Substances Data)

Upstream product

• 451-40-1 phenyl benzyl ketone 
• 1635-61-6 5-chloro-2-nitroaniline 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 5227-55-4 2,3-diphenyl quinoxaline N-oxide 
• 98-59-9 p-toluenesulfonyl chloride 
• 151-50-8 potassium cyanide 
• 98-88-4 benzoyl chloride 
• 7677-24-9 trimethylsilyl cyanide 
• 67-56-1 methanol 
• 76672-25-8 2,6-Dichloro-3-phenylquinoxaline 
• 98-80-6 phenylboronic acid 
• 492-70-6 1,2-diphenyl-1,2-ethanediol 
• 501-65-5 diphenyl acetylene 
• 95-83-0 4-Chloro-1,2-phenylenediamine 

Downstream Products

• 1582317-83-6 (2-(7-chloro-3-phenylquinoxalin-2-yl)phenyl)(phenyl)methanone 
• 1582317-82-5 (2-(6-chloro-3-phenylquinoxalin-2-yl)phenyl)(phenyl)methanone 

Relevant articles and documents

Tungstophosphoric acid/mesoporous silicas as suitable catalysts in quinoxaline synthesis

Quinoxalines and their derivatives are of great value in the chemical and biological sciences. These compounds are found in dyes, agrochemicals, and are used as building blocks of drugs for the treatment of different diseases. Quinoxalines and their deriv

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

Ruthenium?p-cymene complexes with acylthiourea, and its heterogenized form on graphene oxide act as catalysts for the synthesis of quinoxaline derivatives

Synthesis of a series of half-sandwich Ru(II) complexes (1-5) containing acylthiourea ligand is reported herein. All the Ru(II) complexes were well characterized by analytical and spectroscopic (UV-Vis, FT-IR, NMR and mass spectrometry) methods. Molecular structures of two (2 and 3) of the complexes were confirmed by single crystal X-ray diffraction, and the complexes adopted pseudo-octahedral geometry around Ru. Catalytic ability of the Ru complexes was evaluated in the synthesis of quinoxaline compounds from various 2-nitroaniline and hydroxy ketone derivatives via transfer hydrogenation approach. Active homogeneous catalyst was heterogenized by supporting it on graphene oxide, and the heterogeneous equivalent was characterized by Raman, XPS, TEM, SEM and ICP-OES techniques. Activity of the heterogeneous catalyst was tested, and it can be reused up to five cycles without any loss in activity.