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MSE PRO (2-Butenyl)chloropalladium dimer, ≥98.0% Purity– MSE Supplies LLC

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MSE PRO (2-Butenyl)chloropalladium dimer, ≥98.0% Purity - MSE Supplies LLC

MSE PRO (2-Butenyl)chloropalladium dimer, ≥98.0% Purity

SKU: CM1419

  • $ 12995


MSE PRO™ (2-Butenyl)chloropalladium dimer, ≥98.0% Purity

MSE PRO™ (2-Butenyl)chloropalladium dimer finds extensive use as a catalyst in various cross-coupling reactions, which are fundamental carbon-carbon bond-forming processes in organic synthesis. Some key applications include:

  • Suzuki-Miyaura coupling
  • Heck reaction
  • Sonogashira coupling
  • Negishi coupling
  • Buchwald-Hartwig amination

These reactions are widely employed in the pharmaceutical, agrochemical, and materials science industries for the synthesis of complex organic molecules.

MSE Supplies offers various catalysts and ligands of coupling reaction. Please contact us for customization or bulk orders.

Technical Specifications:

CAS No. 12081-22-0
Chemical name (2-Butenyl)chloropalladium dimer
Synonym(s)
  • Crotylpalladiumchloridedimer
  • Dichlorobis(1-methylallyl)dipalladium
Chemical formula C8H14Cl2Pd2
Pack size 1 g (CM1419)
Molecular weight 393.94 g/mol
Purity ≥98.0%
Melting point 133-140 °C
Appearance Light yellow to green yellow (Solid)
Storage temperature 2-8°C, protect from light, stored under nitrogen

References:

[1] Reek, J. N., de Groot, D., Oosterom, G. E., Kamer, P. C., & van Leeuwen, P. W. (2003). Phosphine-functionalized dendrimers for transition-metal catalysis. Comptes Rendus Chimie6(8-10), 1061-1077.

[2] Reek, J. N., De Groot, D., Oosterom, G. E., Kamer, P. C., & Van Leeuwen, P. W. (2002). Core and periphery functionalized dendrimers for transition metal catalysis; a covalent and a non-covalent approach. Reviews in Molecular Biotechnology90(3-4), 159-181.