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Home  > Palladium, dichloro[1,1'-(9,9-dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine-κP]]-, (SP-4-2)-

AB06050

205319-10-4 | Palladium, dichloro[1,1'-(9,9-dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine-κP]]-, (SP-4-2)-

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $19.00 $13.00 -   +
1g 98% in stock $33.00 $23.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB06050
Chemical Name: Palladium, dichloro[1,1'-(9,9-dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine-κP]]-, (SP-4-2)-
CAS Number: 205319-10-4
Molecular Formula: C39H32Cl2OP2Pd
Molecular Weight: 755.9443
MDL Number: MFCD14155707
SMILES: CC1(C)c2cccc3c2Oc2c1cccc2[P+]([Pd-2]([P+]3(c1ccccc1)c1ccccc1)(Cl)Cl)(c1ccccc1)c1ccccc1

 

Computed Properties
Complexity: 734  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 45  
Hydrogen Bond Acceptor Count: 1  
Rotatable Bond Count: 6  

 

 

Upstream Synthesis Route
  • Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II) is a versatile and highly effective catalyst widely used in chemical synthesis. It plays a crucial role in various organic transformations, particularly in cross-coupling reactions.This palladium complex is known for its exceptional reactivity and selectivity in facilitating C-C and C-heteroatom bond formations. It serves as a key component in Suzuki-Miyaura coupling, Heck coupling, Sonogashira coupling, and other important reactions in organic chemistry.By promoting these coupling reactions, this palladium catalyst enables the efficient construction of complex molecular structures with high precision and yield. Its ability to catalyze various carbon-carbon and carbon-heteroatom bond formations has made it an indispensable tool in the synthesis of pharmaceuticals, agrochemicals, materials, and other valuable organic compounds.
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