1276560-29-2

Upstream product

• 90-59-5 3,5-Dibromosalicylaldehyde 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 1276560-32-7 2-(3,5-dibromo-2-(methoxymethoxy)benzyl)isoindoline-1.3-dione 
• 1276560-33-8 (3,5-dibromo-2-(methoxymethoxy)phenyl)methanamine 
• 1276560-34-9 N-(3,5-dibromo-2-(methoxymethoxy)benzyl)-2-nitrobenzamide 
• 1276560-35-0 N-(3,5-dibromo-2-hydroxybenzyl)-2-nitrobenzamide 
• 1276560-40-7 2-chloro-N-(3,5-dibromo-2-(methoxymethoxy)benzyl)benzamide 
• 1276560-41-8 2-chloro-N-(3,5-dibromo-2-ydroxybenzyl)benzamide 
• 413609-64-0 2,4-dibromo-6-((2-chlorobenzamido)methyl)phenyl 2-nitrobenzoate 
• 1276560-30-5 (3,5-dibromo-2-(methoxymethoxy)phenyl)methanol 
• 1276560-31-6 3,5-dibromo-2-(methoxymethoxy)benzyl methanesulfonate 

Relevant academic research and scientific papers

Synthesis and molecular modeling provide insight into a pseudomonas aeruginosa quorum sensing conundrum

The triphenyl amide/ester 12 was originally reported to be a potent mimic of the natural 3-oxo-dodecanoyl homoserine lactone quorum sensing molecule in Pseudomonas aeruginosa. However, explicit synthesis/chemical characterization was lacking, and a later