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 [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)– 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 [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane, >98% - MSE Supplies LLC

MSE PRO [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane, >98%

SKU: CM1112

  • $ 000

MSE PRO™[1,1′-Bis(diphenylphosphino)ferrocene]

dichloropalladium(II), complex with dichloromethane, >98%

MSE PRO [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane, >98% is frequently used as a catalyst for pharmaceutical and pesticide synthesis. It is also a popular choice for isomerization, as well as transverse coupling reactions including Suzuki, Sonogashira, Heck, Negishi, and Stille couplings. Additionally, it is a valuable resource for processes involving carbonylation, oxidation, and carbon-carbon bond formation.

Technical Specifications:

CAS No. 95464-05-4
MDL No. MFCD00792899
Chemical Name [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane
Synonym(s)
  • Pd(dppf)Cl2 · CH2Cl2
  • Pd(dppf)Cl2 · DCM

  • [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (1:1)
Chemical Formula C35H30Cl4FeP2Pd
Package
  • CM1112: 5g
  • CM1113: 10g
  • CM1114: 25g
  • CM1115: 100g
Molecular Weight 816.64 g/mol
Purity >98%
Melting Point 275-280°C
Appearance Orange-red powder
Storage Room temperature, air and heat sensitive, need to protect from light, stored under nitrogen

Buy various catalysts of coupling reaction at MSE Supplies for the best prices on the market. For bulk orders, please contact us for a quote. 

References 

[1] Cvengroš, Ján, et al. "Electrophilic Activation of Benzaldehydes through ortho Palladation: One‐Pot Synthesis of 3‐Methylene‐indan‐1‐ols through a Domino Allylstannylation/Heck Reaction under Neutral Conditions." Angewandte Chemie 121.33 (2009): 6264-6267.

[2] Monot, Julien, et al. "Suzuki− Miyaura Coupling of NHC− Boranes: A New Addition to the C− C Coupling Toolbox." Organic Letters 11.21 (2009): 4914-4917.

[3] Thiel, Oliver R., et al. "Palladium‐Catalyzed Coupling of Aldehyde‐Derived Hydrazones: Practical Synthesis of Triazolopyridines and Related Heterocycles." Angewandte Chemie 122.45 (2010): 8573-8576.

[4] Chiba, Shunsuke, Yan-Jun Xu, and Yi-Feng Wang. "A Pd (II)-catalyzed ring-expansion reaction of cyclic 2-azidoalcohol derivatives: synthesis of azaheterocycles." Journal of the American Chemical Society 131.36 (2009): 12886-12887.