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[1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) Dichloride Dichloromethane Adduct

[1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) Dichloride Dichloromethane Adduct

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Catalog Number

ACM95464054-3

Product Name

[1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) Dichloride Dichloromethane Adduct

Structure

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CAS

95464-05-4

Product Overview
Usage

Synonyms

Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) Dichloromethane Adduct

IUPAC Name

[1,1-Bis(diphenylphosphino)ferrocene]dichloropalladium(II),complex wi...

Molecular Weight

816.64

Molecular Formula

C34H28Cl2FeP2Pd·CH2Cl2

Purity

Pd ≥13.0%

Density

1 g/cm³

Appearance

orange-red crystals

Exact Mass

823.97400

MDL Number

MFCD00015757

Symbol

GHS07

Application

The [1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) Dichloride Dichloromethane Adduct is an organometallic compound characterized by its distinctive orange-red solid form. It serves a crucial role in various chemical reactions, primarily acting as a noble metal catalyst. This versatile compound is widely employed in the preparation of imidazoles, benzimidazoles, and tetrahydropyrimidines. It functions effectively as a catalyst in numerous coupling reactions, including Suzuki and Stille couplings, as well as the borylation of aryl halides. Additionally, it is instrumental in β-alkyl Suzuki-Miyaura cross-coupling reactions using potassium alkyltrifluoroborates, and serves as a catalyst in modified Negishi couplings. The compound is vital in the synthesis of polyheterocycles through a Pd-catalyzed intramolecular N-arylation/C-H bond activation/aryl-aryl bond-forming domino process and is also used for Stille allylation and the amination of aryl bromides. Its ability to facilitate carbonylation and cross-coupling reactions makes it an indispensable tool in advanced organic synthesis.

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CAS
Size
Purity
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95464-05-4
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Pd ≥13.0%
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