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Home  > 1,4'-Bi-1H-pyrazole, 5-(dicyclohexylphosphino)-1',3',5'-triphenyl-

AA08419

1021176-69-1 | 1,4'-Bi-1H-pyrazole, 5-(dicyclohexylphosphino)-1',3',5'-triphenyl-

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $76.00 $53.00 -   +
1g 97% in stock $257.00 $180.00 -   +
5g 97% in stock $1,179.00 $825.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA08419
Chemical Name: 1,4'-Bi-1H-pyrazole, 5-(dicyclohexylphosphino)-1',3',5'-triphenyl-
CAS Number: 1021176-69-1
Molecular Formula: C36H39N4P
Molecular Weight: 558.6954
MDL Number: MFCD11616511
SMILES: C1CCC(CC1)P(c1ccnn1c1c(nn(c1c1ccccc1)c1ccccc1)c1ccccc1)C1CCCCC1

 

Upstream Synthesis Route
  • 5-(Dicyclohexylphosphino)-1',3',5'-triphenyl-[1,4']-bi-1H-pyrazole is a versatile ligand that finds widespread application in chemical synthesis. This bidentate ligand possesses a unique structure consisting of a biaryl backbone with a phosphine group attached. In coordination chemistry, it forms stable complexes with various metal ions, enabling the selective activation of a wide range of substrates.When used in catalytic processes, this ligand facilitates the formation of homogeneous catalysts that exhibit high activity and selectivity in numerous organic transformations. Its bulky dicyclohexylphosphino groups provide steric protection around the metal center, influencing the reactivity and directing the regioselectivity of the catalyzed reactions.One of the key advantages of using 5-(Dicyclohexylphosphino)-1',3',5'-triphenyl-[1,4']-bi-1H-pyrazole in chemical synthesis is its ability to access challenging reaction pathways that lead to valuable products. Its presence can enhance the efficiency of cross-coupling reactions, hydrogenation processes, and asymmetric transformations, making it a valuable tool for synthetic chemists working in the field of organometallic chemistry.
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