Palladium Catalysts (592)

A palladium catalyst is a catalyst that utilizes palladium, a precious metal, renowned for its high efficiency in catalytic reactions. Due to its valuable properties, palladium is extensively applied across the fields of chemistry, pharmaceuticals, and medicine. The primary applications of palladium catalysts include the following: 1. Hydrogenation Catalyst: Palladium serves as a key hydrogenation catalyst, commonly employed in reactions such as hydrocracking, hydrodeamination, hydrodesulfurization, and hydrodeoxygenation. These processes are integral to industries like petrochemicals, pharmaceuticals, and general chemical manufacturing. 2. Catalytic Reducing Agent: Palladium catalysts facilitate the reduction of organic compounds into corresponding alcohols, aldehydes, ketones, and other derivatives. This application is widely utilized in organic synthesis, pharmaceuticals, and related fields. 3. Catalytic Coupling Agent: Palladium catalysts enhance coupling reactions, including Suzuki coupling, Heck coupling, and Negishi coupling. These reactions are instrumental in synthesizing biologically active compounds and are extensively used in the development of pharmaceuticals, pesticides, and other specialized chemicals.

[(Pd(μ-Cl)(κ(2)-P,C-P(OC6H2-2,4-tBu2)(OC6H3-2,4-tBu2)2))2];2(BIS(2 4DI-T-BU-PHENOXY)PHOSPHINOOXY)3;bis[2-(bis(2,4-di-tert-butylphenoxy)phosphino-κp-oxy)-3,5-di-tert-butylphenyl-κc]di-μ-chloro-dipalladium;di-chlorobis(tri(2,4-di-tert-butylphenyl)phosphite-2-C,P)dipalladium(II)  Suzuki  and  Stille  couplings  of  aryl  bromides  and  iodides.;Bedford  Catalyst,  Bis[2-(bis(2,4-di-tert-butylphenoxy)phosphino-KP-oxy)-3,5-di-tert-butylphenyl-KC]di--chloro-dipalladium;di-.mu.-chlorobis(tri(2,4-di-tert-butylphenyl)phosphite-2-C,P)dipalladium (II);[2-bis(2,4-ditert-butylphenoxy)phosphanyloxy-3,5-ditert-butyl-phenyl]-chloro-palladium;di-chlorobis(tri(2,4-di-tert-butylphenyl)phosphite-2 structure diagram

[(Pd(μ-Cl)(κ(2)-P,C-P(OC6H2-2,4-tBu2)(OC6H3-2,4-tBu2)2))2];2(BIS(2 4DI-T-BU-PHENOXY)PHOSPHINOOXY)3;bis[2-(bis(2,4-di-tert-butylphenoxy)phosphino-κp-oxy)-3,5-di-tert-butylphenyl-κc]di-μ-chloro-dipalladium;di-chlorobis(tri(2,4-di-tert-butylphenyl)phosphite-2-C,P)dipalladium(II) Suzuki and Stille couplings of aryl bromides and iodides.;Bedford Catalyst, Bis[2-(bis(2,4-di-tert-butylphenoxy)phosphino-KP-oxy)-3,5-di-tert-butylphenyl-KC]di--chloro-dipalladium;di-.mu.-chlorobis(tri(2,4-di-tert-butylphenyl)phosphite-2-C,P)dipalladium (II);[2-bis(2,4-ditert-butylphenoxy)phosphanyloxy-3,5-ditert-butyl-phenyl]-chloro-palladium;di-chlorobis(tri(2,4-di-tert-butylphenyl)phosphite-2

ACTRMK350

217189-40-7

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Dichloro[1,1'-bis(dicyclohexylphosphiNA)ferrocene]palladiuM (II);[1,1′-Bis(di-cyclohexylphosphino)ferrocene]dichloropalladiuM(II);Dichloro[1,1'-bis(dicyclohexylphosphino)ferrocene]palladium (II);PalladiuM, [1,1'-bis(dicyclohexylphosphino-κP)ferrocene]dichloro-, (SP-4-2)-;Dichloro [1,1'-bis(dicyclohexy;PdCl2(dcypf);Dichloro[1,1'-bis(dicyclohexylphosphino)ferrocene]palladium(II), dichloromethane adduct, 99%;1,1′-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride 98% structure diagram

Dichloro[1,1'-bis(dicyclohexylphosphiNA)ferrocene]palladiuM (II);[1,1′-Bis(di-cyclohexylphosphino)ferrocene]dichloropalladiuM(II);Dichloro[1,1'-bis(dicyclohexylphosphino)ferrocene]palladium (II);PalladiuM, [1,1'-bis(dicyclohexylphosphino-κP)ferrocene]dichloro-, (SP-4-2)-;Dichloro [1,1'-bis(dicyclohexy;PdCl2(dcypf);Dichloro[1,1'-bis(dicyclohexylphosphino)ferrocene]palladium(II), dichloromethane adduct, 99%;1,1′-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride 98%

ACUJPM320

917511-90-1

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Total: 189