Di-mu-chlorobis[5-chloro-2-[(4-chlorophenyl)(hydroxyimino-kappaN)methyl]phenyl-kappaC]palladium dimer, 97%

Code: 668923-1G D2-231

Application

Highly effective catalyst for multiple aryl vinylation via Heck coupling. Palladacycle catalyst employed in a variety of carbon-carbon bond forming reactions.

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Your Price
£183.00 1G
Discontinued
£219.60 inc. VAT

Application

Highly effective catalyst for multiple aryl vinylation via Heck coupling. Palladacycle catalyst employed in a variety of carbon-carbon bond forming reactions.

Catalyst for: Suzuki coupling Suzuki-Miyaura coupling Najera palladacycle-catalyzed intermolecular Heck reaction of Morita-Baylis-Hillman adducts Hiyama cross-coupling Palladium-catalyzed acylation of terminal alkynes with acid chlorides Copper and amine free Sonogashira coupling reaction

Packaging

1 g in glass bottle

250 mg in glass bottle

assay97%
formsolid
InChI keyGIMFEGPTUHULMU-VAABLSLRSA-L
InChI1S/2C13H8Cl2NO.2ClH.2Pd/c2*14-11-5-1-9(2-6-11)13(16-17)10-3-7-12(15)8-4-10;;;;/h2*1-3,5-8,17H;2*1H;;/q;;;;2*+1/p-2/b2*16-13+;;;;
Quality Level100
reaction suitabilityreaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Hiyama Coupling, reaction type: Heck Reaction, reaction type: Sonogashira Coupling, reaction type: Suzuki-Miyaura Coupling, core: palladium, reaction type: Negishi Coupling, reaction type: Stille Coupling, reagent type: catalyst
SMILES stringON=C(/c1ccc(Cl)cc1)c2ccc(Cl)cc2[Pd]Cl.ON=C(/c3ccc(Cl)cc3)c4ccc(Cl)cc4[Pd]Cl
Cas Number287410-78-0
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