161744-27-0

Upstream product

• 161744-28-1 10-(4-tert-butylphenyl)-3-<2-(trifluoromethyl)phenyl>pyrimido<4,5-b>quinoline-2,4(3H,10H)-dione 
• 161744-26-9 10-(4-tert-butylphenyl)-3-<2-(hydroxymethyl)phenyl>pyrimido<4,5-b>quinoline-2,4(3H,10H)-dione 
• 88-17-5 2-(trifluoromethyl)benzenamine 
• 185435-31-8 6-(4-tert-Butyl-phenylamino)-3-(2-trifluoromethyl-phenyl)-1H-pyrimidine-2,4-dione 
• 185435-29-4 1-(2-(trifluoromethyl)phenyl)pyrimidine-2,4,6-trione 
• 185435-30-7 6-Chloro-3-(2-trifluoromethyl-phenyl)-1H-pyrimidine-2,4-dione 
• 13114-85-7 1-<2-(trifluoromethyl)phenyl>urea 
• 769-92-6 4-tert-Butylaniline 
• 185435-32-9 2-[10-(4-tert-Butyl-phenyl)-2,4-dioxo-4,10-dihydro-2H-pyrimido[4,5-b]quinolin-3-yl]-benzoic acid 

Downstream Products

• 161744-26-9 10-(4-tert-butylphenyl)-3-<2-(hydroxymethyl)phenyl>pyrimido<4,5-b>quinoline-2,4(3H,10H)-dione 

Relevant academic research and scientific papers

Variation of reaction channel in. A flavoenzyme model with a modified pyrimidine ringe

A chiral 5-deazaflavin derivative with 2-hydroxymethylphenyl group at N(3) position of the pyrimidine ring has been synthesized. Oxidized form of the 5-deazaflavin derivative is reduced stereospecifically: the hydroxymethyl group exerts steric inhibition

Atropisomeric flavoenzyme models with a modified pyrimidine ring: Syntheses, physical properties, and stereochemistry, in the reactions with NAD(P)H analogs

Optically active 5-deazaflavin derivatives (3-aryl-10-(4-tert-butylphenyl)pyrimido[4,5-b]quinoline-2,4(3H,10H)-di one) with an axial chirality at the pyrimidine ring have been synthesized, and the kinetics of enantiomerization have been measured for some