155268-88-5 Usage
Uses
Used in Pharmaceutical Industry:
(4R)-2-Methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine is used as a catalyst in the pharmaceutical industry for its ability to facilitate asymmetric transformations in organic synthesis. This allows for the production of enantiomerically pure compounds, which are essential for the development of many pharmaceuticals with desired biological activities and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, (4R)-2-Methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine serves as a catalyst to enable the synthesis of chiral agrochemicals with improved selectivity and reduced environmental impact. (4R)-2-Methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine's ability to promote asymmetric reactions ensures the production of target molecules with desired biological properties and minimal off-target effects.
Used in Fine Chemicals Production:
(4R)-2-Methyl-4,5,5-triphenyl-1,3,2-oxazaborolidine is utilized as a catalyst in the production of fine chemicals, where the synthesis of enantiomerically pure compounds is crucial for various applications, such as fragrances, flavors, and specialty materials. Its unique stereochemistry and catalytic properties contribute to the efficient and selective synthesis of these high-value chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 155268-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,2,6 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155268-88:
(8*1)+(7*5)+(6*5)+(5*2)+(4*6)+(3*8)+(2*8)+(1*8)=155
155 % 10 = 5
So 155268-88-5 is a valid CAS Registry Number.
155268-88-5Relevant academic research and scientific papers
Parsons, Philip J.,Pennicott, Lewis,Eshelby, James,Goessman, Matthias,Highton, Adrian,Hitchcock, Peter
, p. 9387 - 9390 (2007)
(Chemical Equation Presented) An ester enolate rearrangement/silicon mediated fragmentation cascade was used to convert 7 and 8 into the alcohol 9. The alcohol 9 was converted into the allylic alcohol 12 and then to the ester 14. A further ester enolate r
