CAS 12107-56-1
:Dichloro[(1,2,5,6-η)-1,5-cyclooctadiene]palladium
Description:
Dichloro[(1,2,5,6-η)-1,5-cyclooctadiene]palladium, with the CAS number 12107-56-1, is a coordination compound featuring palladium as the central metal atom. This compound is characterized by its palladium(II) oxidation state and the presence of two chloride ligands and a cyclooctadiene ligand that coordinates to the metal in a η^6 fashion. The cyclooctadiene ligand contributes to the compound's stability and reactivity, making it useful in various catalytic applications, particularly in organic synthesis and cross-coupling reactions. The dichloro substitution enhances the electrophilic nature of the palladium center, facilitating its role as a catalyst. This compound is typically handled under inert atmospheres due to its sensitivity to moisture and air. Its unique structure allows for interesting interactions with other reagents, making it a valuable precursor in the synthesis of more complex organometallic compounds. Overall, dichloro[(1,2,5,6-η)-1,5-cyclooctadiene]palladium is an important compound in the field of organometallic chemistry and catalysis.
Formula:C8H12Cl2Pd
InChI:InChI=1S/C8H12.2ClH.Pd/c1-2-4-6-8-7-5-3-1;;;/h1-2,7-8H,3-6H2;2*1H;/q;;;+2/p-2
InChI key:InChIKey=RRHPTXZOMDSKRS-UHFFFAOYSA-L
SMILES:[Cl-][Pd+2]123([Cl-])[CH]4=[CH]1CC[CH]2=[CH]3CC4
Synonyms:- (1,5-Cyclooctadiene)palladium dichloride
- (1Z,5Z)-cycloocta-1,5-diene
- (1Z,5Z)-cycloocta-1,5-diene - dichloropalladium (1:1)
- 1,5-Cyclooctadiene, palladium complex
- 1,5-Cyclooctadienepalladium(II) Dichloride
- Allylpalladium chloride dimer
- Dichloro(1,5-cyclooctadiene)palladium
- Dichloro(1,5-cyclooctadiene)palladium(II)
- Dichloro(cyclooctadiene)palladium
- Dichloro(η<sup>4</sup>-1,5-cyclooctadiene)palladium
- Dichloro[(1,2,5,6-η)-1,5-cyclooctadiene]palladium
- Dichloropalladium
- NSC 169973
- Palladium, dichloro(1,5-cyclooctadiene)-
- See more synonyms
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Found 7 products.
Dichloro(1,5-cyclooctadiene)palladium(II), 99%
CAS:<p>Dichloro(1,5-cyclooctadiene)palladium(II), 99%</p>Formula:PdCl2C8H12)Purity:99%Color and Shape:yellow xtl.Molecular weight:285.49Cycloocta-1,5-diene; palladium chloride
CAS:Formula:C8H12Cl2PdPurity:98%Color and Shape:SolidMolecular weight:285.5069Dichloro(1,5-cyclooctadiene)palladium(II)
CAS:<p>Dichloro(1,5-cyclooctadiene)palladium(II)</p>Formula:·C8H12·Cl2PdPurity:98%Color and Shape: yellow solidMolecular weight:285.51g/molDichloro(1,5-cyclooctadiene)palladium(II)
CAS:Formula:C8H12Cl2PdPurity:>98.0%(T)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:285.50Dichloro (cycloocta-1,5-dienyl) palladium(II); 99.95% (metals basis)
CAS:Formula:Pd(C8H12)Cl2Molecular weight:285.49Dichloro(1,5-cycloocatadiene)palladium(II)
CAS:Formula:C8H12Cl2PdPurity:95%Color and Shape:SolidMolecular weight:285.5Dichloro(1,5-cyclooctadiene)palladium(II)
CAS:Controlled Product<p>Dichloro(1,5-cyclooctadiene)palladium(II) is a stable metal complex in which the chlorine atom is coordinated to two benzyl groups and one palladium atom. The chloride ion is coordinated to the palladium atom through a strong coordinate bond. The chloride ion is also coordinated to the two benzyl groups by weaker coordinate bonds. In the presence of sodium carbonate, hydrogen chloride and nitrogen gas, dichloro(1,5-cyclooctadiene)palladium(II) reacts with hydrogen chloride to form stable complexes that are soluble in water. These complexes can be used as catalysts for organic reactions because they are able to transfer hydrogen atoms between molecules without breaking covalent bonds. Dichloro(1,5-cyclooctadiene)palladium(II) has been shown to have antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa</p>Formula:C8H12Cl2PdPurity:Min. 98%Molecular weight:285.51 g/mol






