Skip to Content
Merck
All Photos(2)

Key Documents

673064

Sigma-Aldrich

(2-Methylallyl)palladium(II) chloride dimer

Synonym(s):

Chloro(2-methylallyl)palladium(II) dimer, Dichlorobis(2-methylallyl)dipalladium, NSC 270885

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
[CH2=C(CH3)CH2PdCl]2
CAS Number:
Molecular Weight:
393.94
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

form

solid

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

168.2-174.0 °C

storage temp.

2-8°C

SMILES string

Cl[Pd].Cl[Pd].[CH2][C]([CH2])C.[CH2][C]([CH2])C

InChI

1S/2C4H7.2ClH.2Pd/c2*1-4(2)3;;;;/h2*1-2H2,3H3;2*1H;;/q;;;;2*+1/p-2

InChI key

XVIHZVZZPKOMRE-UHFFFAOYSA-L

Application

Catalyst for:
  • Asymmetric allylic alkylation reactions
  • Suzuki-Miyaura reactions
  • Reductive cleavage reactions
  • Reaction of alkenyloxiranes with carbon monoxide

Analysis Note

Precursor to a Pd(I) catalyst used in cross-coupling of organosilanols.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Scott E Denmark et al.
Organic letters, 8(4), 793-795 (2006-02-14)
[reaction: see text] Sodium silanolates derived from a number of heterocyclic silanols undergo cross-coupling with a variety of aromatic iodides and bromides under mild conditions. In situ deprotonation of the silanols with an equivalent amount of sodium hydride in toluene

Articles

Pd-catalyzed cross-coupling of silicon compounds offers an alternative in synthetic chemistry.

Pd-catalyzed cross-coupling of silicon compounds offers an alternative in synthetic chemistry.

Pd-catalyzed cross-coupling of silicon compounds offers an alternative in synthetic chemistry.

Pd-catalyzed cross-coupling of silicon compounds offers an alternative in synthetic chemistry.

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