• נגישות
  • 4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals

    A14462.03
    CAS Number: 5720-07-0See All CAS: 5720-07-0 In Stock

      CAT NUM
      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: A14462.03
      4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals
      Pack Size: 1GR
      PRICE: 
      CAT NUM: A14462.06
      4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals
      Pack Size: 5GR
      PRICE: 
      CAT NUM: A14462.14
      4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 

      CAS Number
      5720-07-0
      Pack Size
      1GR, 5GR, 25GR
      Molecular Formula
      C7 H9 B O3
      Molecular Weight
      151.96
      MFCD
      00039139
      Storage Temp
      RT
      Brand
      Thermo Scientific - Alfa Aesar

      4-Methoxybenzeneboronic acid is used for Suzuki-Miyaura cross-coupling reactions, Pd-catalyzed direct arylation, Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, Palladium-catalyzed stereoselective Heck-type reaction, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence, Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Ruthenium catalyzed direct arylation, Rh-catalyzed asymmetric conjugate addition, Ligand-free copper-catalyzed coupling.

      This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.


      Applications
      4-Methoxybenzeneboronic acid is used for Suzuki-Miyaura cross-coupling reactions, Pd-catalyzed direct arylation, Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, Palladium-catalyzed stereoselective Heck-type reaction, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence, Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Ruthenium catalyzed direct arylation, Rh-catalyzed asymmetric conjugate addition, Ligand-free copper-catalyzed coupling.

      Solubility
      Soluble in dimethyl sulfoxide and methanol.

      Notes
      Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
      Certifications
      Customer service via whatsapp