28488-45-1

Upstream product

• 122-56-5 tributyl borane 
• 89-55-4 5-bromosalicyclic acid 
• 54628-04-5 sodium salt of 4-butyl phenol 
• 119-36-8 methyl salicylate 
• 36481-17-1 2-hydroxy-5-butyryl-benzoic acid methyl ester 
• 106393-53-7 2-hydroxy-5-butyryl-benzoic acid 
• 40523-61-3 2-butyryloxy-benzoic acid methyl ester 

Downstream Products

• 78417-76-2 5-Butyl-2-hydroxy-N-(3-trifluoromethyl-phenyl)-benzamide 
• 78417-63-7 N-(4-Bromo-phenyl)-5-butyl-2-hydroxy-benzamide 

Relevant academic research and scientific papers

B-Alkyl Suzuki-Miyaura cross-coupling of tri-n-alkylboranes with arylbromides bearing acidic functions under mild non-aqueous conditions

An efficient and chemoselective Pd-catalyzed B-alkyl Suzuki-Miyaura cross-coupling of tri-n-alkylboranes with arylbromides possessing acidic functions is described. This protocol features the relatively weak base Cs2CO3 and mild non-

Direct B-alkyl Suzuki-Miyaura cross-coupling of trialkyl-boranes with aryl bromides in the presence of unmasked acidic or basic functions and base-labile protections under mild non-aqueous conditions

An efficient and chemoselective palladium-catalyzed direct B-alkyl Suzuki-Miyaura cross-coupling of trialkylboranes with diversely functionalized aryl bromides is described. A wide variety of unmasked acidic or basic functions are tolerated. The mild non-

Phenyl esters of 4-benzoyloxybenzoic acid

Nematic esters of the formula SPC1 Wherein R1 and R2 are each alkyl, alkoxyalkyl, alkoxy or alkoxyalkoxy of 1 to 10 carbon atoms, X is CN or NO2 and Y is H or X which are useful for influencing the electrooptic properties