Thank you!

Your quote has been successfully submitted!

For products requiring additional information, our team will contact you within 1 business day

Failed

There was an error submitting your quote. Please try again.

MSE PRO Di-MU-iodobis(tri-t-butylphosphino)dipalladium(I)– MSE Supplies LLC

Free Shipping on MSE PRO Online Orders of $500 or More! U.S. Orders Only * Offer Excludes Hazmat Shipments *

Menu
Cart

This product has been added to the cart.

MSE PRO Di-MU-iodobis(tri-t-butylphosphino)dipalladium(I), ≥98.0% Purity - MSE Supplies LLC

MSE PRO Di-MU-iodobis(tri-t-butylphosphino)dipalladium(I), ≥98.0% Purity

SKU: CM1408

  • £58500
  • Save £6500

MSE PRO™ Di-MU-iodobis(tri-t-butylphosphino)dipalladium(I), ≥98.0% Purity

MSE PRO™ Di-MU-iodobis(tri-t-butylphosphino)dipalladium(I) is an organometallic palladium complex, frequently utilized as a catalyst precursor in a range of cross-coupling reactions. It acts as a pre-catalyst for palladium-catalyzed cross-coupling reactions, including Suzuki coupling, Heck reaction, Sonogashira coupling, and Buchwald-Hartwig amination. The versatile compound is extensively used in organic synthesis, pharmaceutical research, and material science applications.

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

Technical Specifications:

CAS No. 166445-62-1
Chemical name Di-MU-iodobis(tri-t-butylphosphino)dipalladium(I)
Synonym(s)
  • Di-μ-iodobis(tri-t-butylphosphino)dipalladium(I)

  • palladium(l) tri-tert-butylphosphine iodide dimer
Chemical formula C24H54I2P2Pd2
Pack size

5 g (CM1408)
Molecular weight 871.28 g/mol
Purity ≥98.0%
Appearance Brown to black solid
Storage temperature 2-8°C, protect from light, stored under nitrogen

References:

[1] Ishita, K. (2017). Design, Synthesis and Evaluation of Carborane and Thiazole Derivatives. The Ohio State University.

[2] Denmark, S. E., & Ober, M. H. (2004). Palladium‐Catalyzed Cross‐Coupling Reactions of Substituted Aryl (dimethyl) silanols. Advanced Synthesis & Catalysis, 346(13‐15), 1703-1714.