62107-95-3

Upstream product

• 17628-76-1 p-tolylglyoxalmonoxime 
• 13664-98-7 2,2-dibromo-1-(4-methylphenyl)ethanone 
• 1075-47-4 4-methylphenylglyoxal 
• 22027-51-6 3-oxo-3-p-tolyl-propionic acid methyl ester 

Downstream Products

• 69810-75-9 1-{4-methylphenyl}-ethylenediamine 
• 29945-56-0 2-oxy-4-p-tolyl-furazan-3-ylamine 
• 86329-42-2 4-p-tolyl-furazan-2-oxide 
• 86329-45-5 3-p-tolyl-furazan-2-oxide 
• 91600-48-5 benzoyloxyimino-p-tolyl-acetonitrile 
• 30016-27-4 4-amino-3-(4-tolyl)furoxan 

Relevant academic research and scientific papers

One-pot synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans

A "one pot" method for the synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans from β-aryl- and 4-β-hetaryl-β-oxo acid esters was developed.

The Oxidation of 6- and 7-Aryl-4(3H)-pteridinones by Immobilized Arthrobacter M-4 Cells Containing Xanthine Oxidase

The preparation of 6- and 7-(pX-phenyl)-4(3H)-pteridinones (X = H, CH3, OCH3) is described.The oxidation of these compounds by (immobilized) Arthrobacter M-4 cells containing xanthine oxidase has been studied.The oxidation monitored by uv spectroscopy usually goes fast, except for 7-(pX-phenyl)-4(3H)-pteridinones (X = CH3, OCH3), which are slowly oxidized.With bacterial cells immobilized in gelatine crosslinked with glutaraldehyde small laboratory-scale oxidations were carried out.Based on spectral data the products of the oxidation reactions are 6- and 7-aryllumazines.