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AB52021

172418-32-5 | Catacxium(r) c

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $33.00 $23.00 -   +
1g 98% in stock $46.00 $33.00 -   +
5g 98% in stock $210.00 $147.00 -   +
10g 98% in stock $417.00 $292.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB52021
Chemical Name: Catacxium(r) c
CAS Number: 172418-32-5
Molecular Formula: C46H50O4P2Pd2
Molecular Weight: 941.6743
MDL Number: MFCD01075746
SMILES: [CH2-]c1ccccc1[PH+](c1ccccc1C)c1ccccc1C.[CH2-]c1ccccc1[PH+](c1ccccc1C)c1ccccc1C.CC(=O)O.CC(=O)O.[Pd].[Pd]

 

Upstream Synthesis Route
  • Trans-Bis(acetato)bis[2-[bis(2-methylphenyl)phosphino]benzyl]dipalladium(II) is a versatile palladium complex widely used in chemical synthesis as a catalyst for various organic transformations. Its unique structure, consisting of palladium atoms coordinated by acetate ligands and phosphine ligands, imparts specific reactivity that enables the facilitation of key reactions in organic chemistry.One significant application of this palladium complex is in the Suzuki-Miyaura cross-coupling reaction, a cornerstone in modern organic synthesis. In this reaction, trans-Bis(acetato)bis[2-[bis(2-methylphenyl)phosphino]benzyl]dipalladium(II) serves as a catalyst, facilitating the coupling of aryl halides with boronic acids to form biaryl compounds. This transformation is invaluable for the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials.Furthermore, the coordination environment of the palladium centers in this complex enhances the stability and efficiency of the catalytic process, allowing for high yields and selectivity in the desired cross-coupling reactions. Its compatibility with a wide range of substrates and functional groups makes it a valuable tool for synthetic chemists seeking to construct carbon-carbon bonds in a controlled and efficient manner.In summary, trans-Bis(acetato)bis[2-[bis(2-methylphenyl)phosphino]benzyl]dipalladium(II) is a powerful catalyst that plays a crucial role in promoting important carbon-carbon bond-forming reactions, thereby enabling the streamlined synthesis of complex organic compounds with diverse applications.
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