64009-05-8

Upstream product

• 1121-74-0 potassium 4-chlorophenoxide 
• 536-38-9 4-chlorobenzoylmethyl bromide 
• 106-48-9 4-chloro-phenol 

Downstream Products

• 1330540-11-8 C₂₃H₁₇Cl₂NO₃ 
• 1330540-09-4 C₂₀H₁₂Cl₂FNO 
• 1330540-07-2 C₂₁H₁₅Cl₂NO₂ 
• 1330540-03-8 C₂₀H₁₂BrCl₂NO 
• 1330540-05-0 C₂₀H₁₂Cl₂FNO 
• 1330540-01-6 C₂₀H₁₂Cl₃NO 
• 1330539-99-5 C₂₀H₁₃Cl₂NO 
• 129330-26-3 7-(4-Chloro-phenoxy)-6-(4-chloro-phenyl)-3-p-tolyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 129330-24-1 7-(4-Chloro-phenoxy)-6-(4-chloro-phenyl)-3-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 129330-20-7 7-(4-Chloro-phenoxy)-6-(4-chloro-phenyl)-3-ethyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 129330-12-7 7-(4-Chloro-phenoxy)-6-(4-chloro-phenyl)-3-methyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 100527-46-6 2-bromo-2-(4-chloro-phenoxy)-1-(4-chloro-phenyl)-ethanone 

Relevant academic research and scientific papers

Unprecedented C-2 arylation of indole with diazonium salts: Syntheses of 2,3-disubstituted indoles and their antimicrobial activity

A novel reaction of indole with aryldiazonium salts leading to the formation of 2-aryl-3-(arylazo)indoles was discovered. The products were found to possess potent anti-MRSA and anti-LLVRE activities. The SAR studies indicate that the potentially metaboli

CHEMICAL COMPOUNDS

Compounds of formula (I):wherein variable groups are as defined within; for use in the inhibition of 11betaHSD1 are described