541540-58-3 Usage
Uses
Used in Catalysts:
(2S)-1-[(4S)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene is used as a catalyst in various chemical reactions due to its unique structure and the presence of the diphenylphosphino group, which can facilitate the transfer of phosphorus in catalytic processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2S)-1-[(4S)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene is used as a potential therapeutic agent or as a building block for the synthesis of more complex molecules with medicinal properties. Its unique structure may allow it to interact with biological targets in novel ways.
Used in Materials Science:
(2S)-1-[(4S)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene is used in the development of new materials, such as in the synthesis of polymers or the creation of new metal-organic frameworks, where its ferrocene core and other functional groups can contribute to the desired material properties.
Used in Analytical Chemistry:
In analytical chemistry, (2S)-1-[(4S)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene can be used as a chiral selector or a recognition element in the development of sensors or chromatographic methods for the separation and detection of enantiomers. Its stereochemistry and functional groups may provide selectivity in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 541540-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,1,5,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 541540-58:
(8*5)+(7*4)+(6*1)+(5*5)+(4*4)+(3*0)+(2*5)+(1*8)=133
133 % 10 = 3
So 541540-58-3 is a valid CAS Registry Number.
541540-58-3Relevant academic research and scientific papers
Kinetic resolution of racemic ferrocenylphosphine compounds by enantioselective oxidation using cyclic selenoxides having a chiral ligand
Miyake, Yoshihiro,Yamauchi, Akiyoshi,Nishibayashi, Yoshiaki,Uemura, Sakae
, p. 381 - 387 (2007/10/03)
Cyclic selenoxides having an optically active binaphthyl skeleton work as the reagents for enantioselective oxidation of phosphines to the corresponding phosphine oxides. Treatment of a racemic 2-oxazolin-2-ylferrocenylphosphine with one of the selenoxides in carbon tetrachloride in the presence of phenol affords the corresponding phosphine oxide together with the unreacted starting phosphine, both with moderate enantioselectivities (the phosphine oxide, up to 13% ee; the phosphine, up to 29% ee).
