935684-39-2

Upstream product

• 150-76-5 4-methoxy-phenol 
• 935-50-2 4,4-dimethoxycyclohexa-2,5-dienone 
• 4301-14-8 acetylenemagnesium bromide 

Downstream Products

• 935684-45-0 methyl 3-(4-((2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)-1H-indol-1-yl)sulfonyl)phenyl) propanoate 
• 935684-46-1 C₂₄H₂₀FNO₆S 
• 1227420-71-4 4-hydroxy-4-(1-tosyl-1H-1,2,3-triazol-4-yl)cyclohexa-2,5-dienone 
• 1227420-72-5 4-hydroxy-4-(1-(4-methoxyphenylsulfonyl)-1H-1,2,3-triazol-4-yl)cyclohexa-2,5-dienone 
• 1227420-85-0 4-hydroxy-4-(1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl)cyclohexa-2,5-dienone 
• 1227420-69-0 4-hydroxy-4-(1-((2R,3S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-1H-1,2,3-triazol-5-yl)cyclohexa-2,5-dienone 
• 1227420-86-1 4-(1-decyl-1H-1,2,3-triazol-4-yl)-4-hydroxycyclohexa-2,5-dienone 
• 1227420-80-5 4-hydroxy-4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,3-triazol-4-yl)cyclohexa-2,5-dienone 
• 1227420-78-1 4-(1-(4-fluorophenyl)-1H-1,2,3-triazol-4-yl)-4-hydroxycyclohexa-2,3-dienone 
• 1227420-77-0 4-(1-(4-bromophenyl)-1H-1,2,3-triazol-4-yl)-4-hydroxycyclohexa-2,5-dienone 
• 1227420-79-2 4-hydroxy-4-(1-(3-(trifluoromethyl)phenyl)-1H-1,2,3-triazol-4-yl)cyclohexa-2,5-dienone 

Relevant academic research and scientific papers

Quinol derivatives as potential trypanocidal agents

Quinols have been developed as a class of potential anti-cancer compounds. They are thought to act as double Michael acceptors, forming two covalent bonds to their target protein(s). Quinols have also been shown to have activity against the parasite Trypa

Quinols as novel therapeutic agents. 7. Synthesis of antitumor 4-[1-(arylsulfonyl-1H-indol-2-yl)]-4-hydroxycyclohexa-2,5-dien-1-ones by Sonogashira reactions

Interaction of 2-iodoaniline or 5-fluoro-2-iodoaniline with a range of arylsulfonyl chlorides affords sulfonamides that undergo Sonogashira couplings under thermal or microwave conditions with the alkyne 4-ethynyl-4- hydroxycyclohexa-2,5-dien-1-one follow