225657
Bis(acetonitrile)dichloropalladium(II)
99%
Synonym(s):
Palladium(II) chloride diacetonitrile complex
About This Item
Recommended Products
assay
99%
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
greener alternative product characteristics
Catalysis
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sustainability
Greener Alternative Product
greener alternative category
, Aligned
SMILES string
CC#N.CC#N.Cl[Pd]Cl
InChI
1S/2C2H3N.2ClH.Pd/c2*1-2-3;;;/h2*1H3;2*1H;/q;;;;+2/p-2
InChI key
RBYGDVHOECIAFC-UHFFFAOYSA-L
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General description
Application
On the Way Towards Greener Transition-Metal-Catalyzed Processes as Quantified by E Factors
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Certificates of Analysis (COA)
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A variety of palladium-catalyzed cross-coupling reactions can be run under room temperature conditions in water with TPGS- 750-M, using a variety of commercially available palladium complexes and ligands.
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