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[2',4'-Bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexylphosphine is a complex organic compound with a unique molecular structure. It is characterized by its two cyclohexylphosphine groups connected to a biphenyl core, which is further substituted with two 1,1-dimethylethyl groups at the 2' and 4' positions, and a methoxy group at the 6' position. [2',4'-Bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexylphosphine is known for its potential applications in various chemical reactions and processes due to its unique structural features and reactivity.

1848244-75-6

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1848244-75-6 Usage

Uses

Used in Pharmaceutical Industry:
[2',4'-Bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexylphosphine is used as a ligand in the pharmaceutical industry for the development of novel drugs and therapeutic agents. Its unique structural features and reactivity enable it to form stable complexes with various metal ions, which can be utilized in the design and synthesis of new pharmaceutical compounds.
Used in Chemical Synthesis:
In the field of chemical synthesis, [2',4'-Bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexylphosphine is used as a versatile ligand for various palladium-catalyzed reactions. Its application in the micellar aqueous Negishi coupling of heterocyclic alkyl bromides, as developed by the Buchwald group, offers best-in-class performance. This ligand's ability to form stable complexes with palladium ions allows for efficient and selective coupling reactions, leading to the formation of a wide range of valuable synthetic products.
Used in Material Science:
[2',4'-Bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexylphosphine can also be employed in the field of material science, where its unique structural features and reactivity can be utilized for the development of new materials with specific properties. For example, its ability to form stable complexes with metal ions can be exploited in the design of novel catalysts, sensors, or other functional materials with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1848244-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,4,8,2,4 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1848244-75:
(9*1)+(8*8)+(7*4)+(6*8)+(5*2)+(4*4)+(3*4)+(2*7)+(1*5)=206
206 % 10 = 6
So 1848244-75-6 is a valid CAS Registry Number.

1848244-75-6Downstream Products

1848244-75-6Relevant academic research and scientific papers

An Improved System for the Aqueous Lipshutz-Negishi Cross-Coupling of Alkyl Halides with Aryl Electrophiles

Bhonde, Vasudev R.,O'Neill, Brian T.,Buchwald, Stephen L.

, p. 1849 - 1853 (2016)

The development of a palladacyclic precatalyst supported by a new biaryl(dialkyl)phosphine ligand (VPhos) in combination with octanoic acid/sodium octanoate as a simple and effective surfactant system provided an improved catalyst system for the rapid con

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