Palladium (592)

A palladium catalyst is a catalyst that utilizes palladium, a precious metal, known for its high efficiency in catalytic reactions. Due to its remarkable properties, palladium is extensively applied in chemistry, pharmacy, and medicine. The main applications of palladium catalysts include the following: 1. Hydrogenation Catalyst: Palladium serves as a key hydrogenation catalyst, commonly employed in processes such as hydrocracking, hydrodeamination, hydrodesulfurization, and hydrodeoxygenation. These reactions are integral to industries like petrochemicals, pharmaceuticals, and chemicals. 2. Catalytic Reducing Agent: Palladium catalysts are capable of reducing organic compounds into corresponding alcohols, aldehydes, ketones, and other derivatives. This ability makes them highly valuable in organic synthesis, pharmaceuticals, and related fields. 3. Catalytic Coupling Agent: Palladium catalysts facilitate coupling reactions, including Suzuki coupling, Heck coupling, and Negishi coupling. These reactions enable the synthesis of compounds with significant biological activities, finding widespread use in the production 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