2449-19-6

Upstream product

• 106-37-6 1.4-dibromobenzene 
• 2425-81-2 phen-1,4-ylenbis(magnesiumbromid) 
• 4612-26-4 1,4-Phenyldiboronic acid 
• 71-36-3 butan-1-ol 

Downstream Products

• 71258-12-3 1,4-bis(dichloroboryl)benzene 
• 109-69-3 n-Butyl chloride 
• 10025-87-3 trichlorophosphate 
• 4612-26-4 1,4-Phenyldiboronic acid 
• 177343-51-0 2,2'-p-phenylene bis(4-diphenylphosphino)-4H-1,3-dioxa-2-boraphenanthrene 
• 177343-50-9 2,2'-p-phenylene bis(4-diphenylphosphino)-1,3,2-benzodioxaborinane 
• 177343-52-1 p-phenylene bis[4-(diphenylphosphinoyl)-1,3,2-benzodioxaborinane] 

Relevant academic research and scientific papers

Synthesized of bore-subphthalocyanine chloride from 1,4-benzene diboronic acid

SubPcBCl is synthesized from 1,4-benzene diboronic acid with a yield of 45%. The infrared, electronic and proton NMR spectra are in accordance with the results of literature.

Reaction of Arylboronic Acids and their Derivatives with Lead Tetra-acetate. The Generation of Aryl-lead Triacetates, and meta- and para-Phenylenebis(lead triacetate), in situ for Electrophilic Arylation

Arylboronic acids and some of their derivatives have been found to undergo a rapid boron-lead exchange with lead tetra-acetate.In the presence of a catalytic amount of mercury(II) acetate, the reaction produces mainly the aryl-lead triacetate, and it has been developed as a convenient method for in situ generation of these useful electrophilic C-arylating reagents.The reaction allows the generation for the first time of meta- and para-phenylenebis(lead triacetate), compounds which behave as meta- and para-phenylene dication equivalents.