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Structure of 114757-66-3
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Bis(acetonitrile)palladium(II) p-toluenesulfonate delivers a stable, moisture-tolerant palladium source for cross-coupling reactions. The acetonitrile ligands facilitate rapid coordination, while the p-toluenesulfonate counterion enhances solubility in polar organic solvents. This reagent integrates seamlessly into Suzuki-Miyaura and Heck reaction protocols under standard conditions.
Bis(acetonitrile)palladium(II) p-toluenesulfonate serves as a reliable, bench-stable source of Pd(II) for catalytic cross-coupling reactions. It facilitates efficient C–C and C–heteroatom bond formations under mild conditions, with the p-toluenesulfonate counterion enhancing solubility and reactivity in polar solvents. The acetonitrile ligands enable rapid ligand exchange, making it well-suited for Suzuki-Miyaura, Stille, and Heck-type transformations. Its stability and ease of handling make it a practical choice for routine synthesis and process development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 3439
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301+H311+H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: