AiFChem
Cart

Recently Added

No recently added products.

Only display the lastest 5 added Cart

Palladium Compounds (592)

A palladium catalyst is a catalyst that utilizes palladium, a precious metal, known for its high efficiency in catalytic reactions. Due to its exceptional performance, palladium is extensively applied in the fields of chemistry, pharmaceuticals, and medicine. The primary applications of palladium catalysts include the following: 1. Hydrogenation Catalyst: Palladium catalysts play a key role in hydrogenation processes, including hydrocracking, hydrodeamination, hydrodesulfurization, and hydrodeoxygenation. These reactions are pivotal in industries such as 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 capability is widely utilized in organic synthesis and pharmaceutical manufacturing. 3. Catalytic Coupling Agent: Palladium catalysts facilitate coupling reactions like Suzuki coupling, Heck coupling, and Negishi coupling. These reactions are instrumental in synthesizing compounds with significant biological activities, making them highly valuable in the production of pharmaceuticals, agrochemicals, and other specialized fields.

[(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

Login to see price

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

Login to see price

Total: 189