52122-46-0

Upstream product

• 23464-45-1 6-(4-methoxyphenyl)-hexyl bromide 
• 7424-54-6 3,5-heptanedione 
• 64431-79-4 4-(6-bromohexyl)phenol 
• 52122-45-9 4-[6-(4-benzyloxyphenyl)-3-hexenyl]-3,5-heptanedione 
• 52121-86-5 6-(4-methoxyphenyl)-3-hexenyl bromide 
• 57840-61-6 6-bromo-1-(4-methoxyphenyl)-1-hexanone 
• 57840-62-7 6-(4-hydroxyphenyl)hexyl iodide 

Downstream Products

• 62325-84-2 4-morpholin-4-yl-butyric acid 4-(8-oxo-7-propionyl-decyl)-phenyl ester 
• 62325-81-9 4-[6-(4-hydroxyphenyl)hexyl]-3,5-heptanedione 3,4,5-trimethoxybenzoate 
• 62325-80-8 3,5-Dimethoxy-benzoic acid 4-(8-oxo-7-propionyl-decyl)-phenyl ester 

Relevant academic research and scientific papers

Aryl substituted diketones

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester.

Methylenedioxyphenyl substituted aliphatic diketones

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester.

Antivital activity of some β diketones. I. Aryl alkyl diketones. In vitro activity against both RNA and DNA viruses

The discovery that 4 [3 ethyl 6 [(3,4 methylenedioxy)phenyl] 3 hexenyl] 3,5 heptanedione exhibited an in vitro inhibitory effect against equine rhinovirus led to a structure activity study to establish the criteria for optimum activity. Modification of th