700045
(2-Butenyl)chloropalladium dimer
≥97%
Synonym(s):
Bis[(1,2,3-η)-2-buten-1-yl]di-μ-chlorodi-palladiumdi-π-crotylpalladium chloride, Di-π-Crotylpalladium chloride, Di-2-butenyldipalladium dichloride, Dichlorobis(1-methylallyl)dipalladium
About This Item
Recommended Products
Quality Level
Assay
≥97%
form
powder
reaction suitability
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
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
mp
133-140 °C
SMILES string
C\C=C\C[Pd]Cl.C\C=C\C[Pd]Cl
InChI
1S/2C4H7.2ClH.2Pd/c2*1-3-4-2;;;;/h2*3-4H,1H2,2H3;2*1H;;/q;;;;2*+1/p-2/b2*4-3+;;;;
InChI key
NTFUUQYNUUTALG-HYTOEPEZSA-L
Application
- Enantioselective elimination of palladium hydride
- Non-covalent anchoring of catalysts to silica supports
- Allylations of cyanoacetates
- Enantioselective nucleophilic substitutions
Reactant for:
- Allylic alkylation reactions
- Preparation of phosphane-functionalized carbosilane dendrimers
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service