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Merck
CN

692913

Bis[(dicyclohexyl)(4-dimethylaminophenyl)phosphine] palladium(II) chloride

96%

Synonym(s):

(A-caPhos)2 PdCl2

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About This Item

Linear Formula:
(CH3)2NC6H4P(C6H11)2PdCl2P(C6H4N(CH3)2)(C6H11)2
CAS Number:
Molecular Weight:
812.22
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.22
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SMILES string

CN(C)c1ccc(cc1)[PH](C2CCCCC2)(C3CCCCC3)[Pd](Cl)(Cl)[PH](C4CCCCC4)(C5CCCCC5)c6ccc(cc6)N(C)C

InChI

1S/2C20H32NP.2ClH.Pd/c2*1-21(2)17-13-15-20(16-14-17)22(18-9-5-3-6-10-18)19-11-7-4-8-12-19;;;/h2*13-16,18-19H,3-12H2,1-2H3;2*1H;

InChI key

ZVLBDYRPWSIJCO-UHFFFAOYSA-N

assay

96%

form

powder

reaction suitability

core: palladium, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: catalyst
reaction type: Cross Couplings

functional group

phosphine

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Articles

Ligand used to prepare a palladium dichloride catalyst on treatment with PdCl2(COD). The catalyst effectively cross-couples aryl boronic acids with heteroaryl chlorides.

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