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Home > Products >  OLED material Phenylbornic acid CAS No.98-80-6

OLED material Phenylbornic acid CAS No.98-80-6 CAS NO.98-80-6

  • Min.Order: 100 Gram
  • Payment Terms: L/C,T/T
  • Product Details

Keywords

  • OLED materials
  • Phenylboronic acid
  • CAS No.98-80-6

Quick Details

  • ProName: OLED material Phenylbornic acid CAS No...
  • CasNo: 98-80-6
  • Appearance: white powder
  • Application: Perampanel raw material, OLED material...
  • DeliveryTime: Tons goods in stock
  • PackAge: 20kg/drum or on request
  • Port: Tianjin
  • ProductionCapacity: 5 Metric Ton/Month
  • Purity: HPLC>99.0%
  • Storage: keep dry and darkness
  • Transportation: on request
  • LimitNum: 100 Gram

Superiority

the lowest price, 99%min purity, 

our factory has more than 120 set of large-scale reactors which can be used to conduct high temperature, high pressure and ultra low temperature reactions. Our facility has rectification, molecular Short-path distillation and other refining workshop together with a testing room equipped with GC, HPLC and other detecting instruments. 

Details

 

 

 Phenylboronic acid is used in numerous cross coupling reactions. In 1979, Miyarura and Suzuki found a carbon-carbon bond forming reaction (now called a Suzuki reaction) using alkenyl boranes, aryl halides, catalytic Pd(0), and base to produce arylated alkene products. This method was generalized to a route producing biaryls by coupling phenylboronic acid with aryl halides.

       More C-C bond forming processes commonly use phenylboronic acid as a reagent. Alpha-amino acids can be generated using the uncatalyzed reaction between alpha-ketoacids, amines, and phenylboronic acid. Heck-type cross coupling of phenylboronic acid to alkenes and alkynes. This unique C-C bond forming reaction has the ability to couple a terminal olefin with boronic acid using a transition metal catalyst. Aryl azides and nitroaromatics can also be generated using phenylboronic acid.PhB(OH)2 can be used as a protecting group for diols and diamines. Phenylboronic acid can also be regioselectively halodeboronated using aqueous bromine, chlorine, or iodine.

           PhB(OH)2 + Br+ H2O → PhBr + B(OH)3 + HBr 
       Phenylboronic acid is used in biology schemes as receptors and sensors for carbohydrates, antimicrobial agents and enzyme inhibitors, neutron capture therapy for cancer, transmembrane transport, and bioconjugation and labeling of proteins and cell surface.

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