96058-39-8

Upstream product

• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 694-83-7 rac-diaminocyclohexane 
• 501-65-5 diphenyl acetylene 
• 1121-22-8 trans-1,2-Diaminocyclohexane 
• 134-81-6 benzil 
• 64162-07-8 2-amino-cyclohexanecarboxylic acid ethyl ester 
• 34126-95-9 2-aminocyclohexanecarboxamide 

Downstream Products

• 694-83-7 rac-diaminocyclohexane 
• 134-81-6 benzil 
• 1296867-29-2 C₂₄H₂₂N₂O₄ 

Relevant academic research and scientific papers

Efficient synthesis of quinoxalines with hypervalent iodine as a catalyst

Various biologically important quinoxalines were efficiently synthesized in excellent yields via one-pot reaction between 1,2-diaminobenzenes and internal alkynes. The method utilizes inexpensive and readily available hypervalent iodine source, such as (diacetoxyiodo)benzene (PhI(OAc)2) and proved to be a better alternative as compared to expensive transition metal catalysts. Quinoxaline 4i [(2-phenyl-3-(3,4,5-trimethoxy phenyl)quinoxaline)] was evaluated for leukemia cancer cell lines and turned out to be a good candidate.

ORGANOMETALLIC COMPLEX, AND LIGHT-EMITTING DEVICE AND ELECTRONIC APPLIANCE USING THE SAME

In a general formula (1), each of R1 and R2 represents any one of hydrogen, an alkyl group, a halogen group, -CF3, an alkoxy group, and an aryl group. M represents an element that belongs to Group 9 or Group 10. Here, an alkyl group