Di-2-butenyldipalladium dichloride

Catalog Number	ACM12081220-2
CAS	12081-22-0
Structure
Synonyms	Bis[(1,2,3-η)-2-buten-1-yl]di-μ-chlorodi-palladiumdi-π-crotylpalladium chloride
Molecular Weight	393.94
Molecular Formula	C8H14Cl2Pd2
Purity	99%
Appearance	White like powder

Q&A

What is the chemical formula of Di-2-butenyldipalladium dichloride?

The chemical formula of Di-2-butenyldipalladium dichloride is C8H14Cl2Pd2.

What is the molecular weight of Di-2-butenyldipalladium dichloride?

The molecular weight of Di-2-butenyldipalladium dichloride is 393.94.

What is the color of Di-2-butenyldipalladium dichloride?

The color of Di-2-butenyldipalladium dichloride is yellow.

What is the storage temperature recommended for Di-2-butenyldipalladium dichloride?

The recommended storage temperature for Di-2-butenyldipalladium dichloride is under inert gas (nitrogen or Argon) at 2-8°C.

What is the melting point of Di-2-butenyldipalladium dichloride?

The melting point of Di-2-butenyldipalladium dichloride is 133-140 °C.

Why is Di-2-butenyldipalladium dichloride considered air sensitive?

Di-2-butenyldipalladium dichloride is considered air sensitive because it reacts with oxygen in the air.

What are the hazard codes associated with Di-2-butenyldipalladium dichloride?

The hazard code associated with Di-2-butenyldipalladium dichloride is Xi.

What are the safety statements related to Di-2-butenyldipalladium dichloride?

The safety statements related to Di-2-butenyldipalladium dichloride are 26-36/37/39.

What are the risk statements for Di-2-butenyldipalladium dichloride?

The risk statements for Di-2-butenyldipalladium dichloride are 36/37/38.

What are some of the uses of Di-2-butenyldipalladium dichloride?

Some of the uses of Di-2-butenyldipalladium dichloride are as a catalyst for enantioselective elimination of palladium hydride, non-covalent anchoring of catalysts to silica supports, allylations of cyanoacetates, enantioselective nucleophilic substitutions, and as a reactant for allylic alkylation reactions and preparation of phosphane-functionalized carbosilane dendrimers.