40910-67-6

Upstream product

• 21728-07-4 3-methyl-1-phenylpyrazolo<3,4-b>quinoxaline 
• 4711-06-2 (1R,2S,3R)-1-(quinoxalin-2-yl)butane-1,2,3,4-tetraol 
• 100-63-0 phenylhydrazine 
• 95-54-5 1,2-diamino-benzene 
• 881-05-0 3-Methyl-1-phenyl-2-pyrazoline-4,5-dione 
• 66895-34-9 3-[1-(phenylhydrazono)-L-threo-2,3,4-trihydroxybut-1-yl]quinoxalin-2(1H)one 
• 68667-54-9 3-(1-phenylhydrazono-D-erythro-2,3,4-trihydroxybut-1-yl)quinoxalin-2-one 
• 40910-70-1 3-(L-threo-glycerol-1-yl)-1-phenyl-pyrazolo[3,4-b]quinoxaline 
• 17460-16-1 1-phenyl-3-(D-erythro-trihydroxypropyl)-1H-pyrazolo[3,4-b]quinoxaline 

Downstream Products

• 107947-74-0 1-Phenyl-3-((Z)-2-pyridin-2-yl-vinyl)-1H-pyrazolo[3,4-b]quinoxaline 
• 33920-28-4 1-phenyl-1H-pyrazolo<3,4-b>quinoxaline 
• 109179-58-0 1-phenyl-3-(1-pyrrolidylmethyl)-1H-pyrazolo<3,4-b>quinoxaline 
• 109179-57-9 3-chloromethyl-1-phenyl-1H-pyrazolo<3,4-b>quinoxaline 
• 113314-14-0 ethyl 1-phenyl-1H-pyrazolo<3,4-b>quinoxaline-3-propanoate 
• 113314-12-8 1-phenyl-1H-pyrazolo<3,4-b>quinoxaline-3-Z-propenoic acid 
• 68636-60-2 3-hydroxymethyl-1-phenyl-1H-pyrazolo<3,4-b>quinoxaline 
• 113314-13-9 (E)-3-(1-Phenyl-1H-pyrazolo[3,4-b]quinoxalin-3-yl)-acrylic acid ethyl ester 
• 107947-76-2 1-Phenyl-3-((Z)-2-quinolin-2-yl-vinyl)-1H-pyrazolo[3,4-b]quinoxaline 
• 109002-31-5 1-phenyl-1H-pyrazolo<2,3-b>quinoxaline-3-carboxylic acid 

Relevant academic research and scientific papers

MAOS of quinoxalines, conjugated pyrazolylquinoxalines and fused pyrazoloquinoxalines from L-ascorbic and D-isoascorbic acid

Microwave-assisted organic synthesis (MAOS) has been used to accelerate the conversion of L-ascorbic acid (1) and D-isoascorbic acid (2) to the title heterocycles by conversion to 3-(L-threo- or D-erythro-glycerol-1-yl) quinoxaline-2-carboxylic acid o-ami

Quinoxalines XIV. Synthesis, 1H, 13C,15N NMR spectroscopic, and quantum chemical study of 1H-pyrazolo[3,4-b]quinoxalines (flavazoles)

The synthesis of a series of 1H-pyrazolo[3,4-b]quinoxalines (flavazoles) by acylation, alkylation, halogenation, and aminomethylation of the parent compound is reported and their structure is investigated by 1H, 13C, and 15/sup

Synthesis and Biological Activity of Pyrazoloquinoxaline Dimethine Cyanine Dyes

New asymmetrical dimethine cyanines (VIa-f) and their bases (VIIa,b), incorporating pyrazoloquinoxaline moiety or its ethiodide, have been prepared and tested for their antibacterial and fungicidal activities.