1-(2-(Diphenylphosphino)phenyl)-N,N,N-trimethylmethanaminium trifluoromethanesulfonate

96%

  • Product Code: 58998
  CAS:    1373945-21-1
Molecular Weight: 483.4835 g./mol Molecular Formula: C₂₃H₂₅F₃NO₃PS
EC Number: MDL Number: MFCD28053547
Melting Point: 154-159°C Boiling Point:
Density: Storage Condition: 2-8℃
Product Description: This chemical is primarily used as a catalyst or ligand in various organic synthesis processes. It plays a significant role in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential for forming carbon-carbon bonds in pharmaceutical and agrochemical production. Its structure, featuring a phosphine group and a quaternary ammonium salt, enhances its stability and reactivity in these reactions. Additionally, it is employed in asymmetric catalysis, contributing to the synthesis of chiral molecules, which are crucial in developing enantiomerically pure drugs. Its trifluoromethanesulfonate counterion further improves its solubility and effectiveness in polar solvents, making it versatile for use in diverse reaction conditions.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.500 10-20 days ฿5,679.00
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1-(2-(Diphenylphosphino)phenyl)-N,N,N-trimethylmethanaminium trifluoromethanesulfonate
This chemical is primarily used as a catalyst or ligand in various organic synthesis processes. It plays a significant role in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are essential for forming carbon-carbon bonds in pharmaceutical and agrochemical production. Its structure, featuring a phosphine group and a quaternary ammonium salt, enhances its stability and reactivity in these reactions. Additionally, it is employed in asymmetric catalysis, contributing to the synthesis of chiral molecules, which are crucial in developing enantiomerically pure drugs. Its trifluoromethanesulfonate counterion further improves its solubility and effectiveness in polar solvents, making it versatile for use in diverse reaction conditions.
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