208671
Bis(triphenylphosphine)palladium(II) dichloride
98%
Quality Level
Assay
98%
form
solid
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
SMILES string
Cl[Pd]Cl.c1(P(c2ccccc2)c3ccccc3)ccccc1.c4(P(c5ccccc5)c6ccccc6)ccccc4
InChI
1S/2C18H15P.2ClH.Pd/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*1-15H;2*1H;/q;;;;+2/p-2
InChI key
YNHIGQDRGKUECZ-UHFFFAOYSA-L
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Related Categories
General description
Application
- Coupling of 2-iodoanisole and terminal alkynes to synthesize 2,3-disubstituted benzofurans.
- Copper-free Sonogashira cross-coupling reaction to synthesize diphenylacetylene.
- Regioselective hydrocarboxylation of styrene.
- Negishi coupling of fluoroarylzinc pivalates to prepare fluorinated oligophenyls.
- Coupling of iodo-α-β-unsaturated esters to afford tetrasubstituted olefins.
related product
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 4 - Skin Sens. 1A
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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What is Product 208671, Bis(triphenylphosphine)palladium(II) dichloride soluble in?
It is soluble in chloroform, toluene, and benzene.
Is Product 208671, Dichlorobis(triphenylphosphine)palladium(II), cis or trans?
We have not specifically tested the material in regards to what isomer it is, however, based on the synthesis of it, it is believed to be predominately trans.
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