921033
Palladium(II) chloride
≥99.99% trace metals basis
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About This Item
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Quality Level
Assay
≥99.99% trace metals basis
mp
678-680 °C (lit.)
density
4 g/mL at 25 °C (lit.)
SMILES string
Cl[Pd]Cl
InChI
1S/2ClH.Pd/h2*1H;/q;;+2/p-2
InChI key
PIBWKRNGBLPSSY-UHFFFAOYSA-L
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Application
Application Guide for Palladium Catalyzed Cross-Coupling Reactions
Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar.
Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar.
Palladium chloride is a transition metal catalyst that can be used to synthesize palladium complexes applicable in heterogeneous catalysis. The Pd NPs synthesized from PdCl2 using oxytocin as a reductant showed remarkable catalytic activity in Suzuki reaction under green conditions.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Met. Corr. 1 - Skin Sens. 1
Storage Class Code
8B - Non-combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Amidoxime modified PAN supported palladium complex: A greener and efficient heterogeneous catalyst for heck reaction.
Inorgorganica Chimica Acta, 502, 119305-119305 (2020)
A simple, efficient and green approach for the synthesis of palladium nanoparticles using Oxytocin: Application for ligand free Suzuki reaction and total synthesis of aspongpyrazine A.
Journal of Organometallic Chemistry, 909, 121093-121093 (2020)
Palladium supported on triazolyl-functionalized hypercrosslinked polymers as a recyclable catalyst for Suzuki?Miyaura coupling reactions
Royal Society of Chemistry Advances, 10(29), 17123-17128 (2020)
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