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(1S)-1-(diphenylphosphino)-2-[(1R)-1-(diphenylphosphino)ethyl]-Ferrocene is a chiral ferrocene-based compound characterized by the presence of two phosphine ligands attached to the cyclopentadienyl rings of the ferrocene unit. (1S)-1-(diphenylphosphino)-2-[(1R)-1-(diphenylphosphino)ethyl]-Ferrocene exhibits a 1S,1R configuration, with the phosphine groups positioned differently around the ferrocene core. Its unique structure and chiral properties render it a valuable asset in the fields of asymmetric catalysis and coordination chemistry, where it can effectively coordinate with transition metals.

155941-31-4

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155941-31-4 Usage

Uses

Used in Asymmetric Catalysis:
(1S)-1-(diphenylphosphino)-2-[(1R)-1-(diphenylphosphino)ethyl]-Ferrocene is utilized as a chiral ligand in asymmetric catalysis for its ability to induce enantioselectivity in various chemical reactions. (1S)-1-(diphenylphosphino)-2-[(1R)-1-(diphenylphosphino)ethyl]-Ferrocene's unique structure and configuration allow it to selectively bind with substrates, facilitating the formation of enantiomerically pure products.
Used in Coordination Chemistry:
In coordination chemistry, (1S)-1-(diphenylphosphino)-2-[(1R)-1-(diphenylphosphino)ethyl]-Ferrocene serves as a versatile ligand for the formation of metal complexes. Its capacity to coordinate with transition metals enables the development of new catalysts and materials with tailored properties for applications in catalysis, sensing, and materials science.
Used in Organic Synthesis:
(1S)-1-(diphenylphosphino)-2-[(1R)-1-(diphenylphosphino)ethyl]-Ferrocene is employed as a reagent or intermediate in organic synthesis, taking advantage of its phosphine functionality and chiral nature. This allows for the synthesis of complex organic molecules with specific stereochemistry, which is crucial in the development of pharmaceuticals and agrochemicals.
Used in Catalysis Research:
As a compound with potential applications in catalysis, (1S)-1-(diphenylphosphino)-2-[(1R)-1-(diphenylphosphino)ethyl]-Ferrocene is used in research to explore new catalytic systems and mechanisms. Its unique structure and properties make it an ideal candidate for studying the role of chirality in catalysis and the development of new catalytic processes.

Check Digit Verification of cas no

The CAS Registry Mumber 155941-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,4 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155941-31:
(8*1)+(7*5)+(6*5)+(5*9)+(4*4)+(3*1)+(2*3)+(1*1)=144
144 % 10 = 4
So 155941-31-4 is a valid CAS Registry Number.

155941-31-4Upstream product

155941-31-4Downstream Products

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