143668-57-9 Usage
Uses
N,N'-[(1S,2S)-1,2-diphenyl-1,2-ethanediyl]bis[2-(diphenylphosphino)-BenzaMide is used as a catalyst in various chemical reactions due to its ability to facilitate and enhance the rate of these reactions. The specific application reasons and industries for its use are as follows:
Used in Chemical Synthesis Industry:
N,N'-[(1S,2S)-1,2-diphenyl-1,2-ethanediyl]bis[2-(diphenylphosphino)-BenzaMide is used as a catalyst for promoting various chemical reactions, such as cross-coupling reactions, hydrogenation, and hydroformylation. Its phosphino and amide groups enable it to coordinate with metal centers, making it an effective catalyst for these processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N'-[(1S,2S)-1,2-diphenyl-1,2-ethanediyl]bis[2-(diphenylphosphino)-BenzaMide is used as a catalyst in the synthesis of complex organic molecules, including those with potential pharmaceutical applications. Its ability to facilitate challenging reactions can lead to the development of new drugs and drug candidates.
Used in Materials Science:
N,N'-[(1S,2S)-1,2-diphenyl-1,2-ethanediyl]bis[2-(diphenylphosphino)-BenzaMide is also utilized in the field of materials science, where it can act as a catalyst in the synthesis of advanced materials with specific properties, such as conductivity, magnetism, or optical activity. Its catalytic properties can help in the development of new materials with potential applications in various industries, including electronics, energy, and aerospace.
Check Digit Verification of cas no
The CAS Registry Mumber 143668-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,6 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143668-57:
(8*1)+(7*4)+(6*3)+(5*6)+(4*6)+(3*8)+(2*5)+(1*7)=149
149 % 10 = 9
So 143668-57-9 is a valid CAS Registry Number.
143668-57-9Relevant academic research and scientific papers
A modular approach for ligand design for asymmetric allylic alkylations via enantioselective palladium-catalyzed ionizations
Trost, Barry M.,Van Vranken, David L.,Bingel, Carsten
, p. 9327 - 9343 (2007/10/02)
A new class of ligands for asymmetric transition metal catalysis based on 2-(diphenylphosphino)benzoic acid was used in a mechanistically-defined palladium-catalyzed reaction in which enantiodifferentiation was the result of selective ionization of substr
