152428-72-3 Usage
Uses
Used in Organic Synthesis:
(4R,5R)-4,5-Dicyclohexyl-2-ethyl-1,3,2-dioxaborolane is utilized as a reagent in organic synthesis for the preparation of various organic compounds, including pharmaceuticals and agrochemicals. Its unique properties and reactivity contribute to the creation of complex organic molecules, making it a crucial component in this field.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4R,5R)-4,5-Dicyclohexyl-2-ethyl-1,3,2-dioxaborolane is used as a key intermediate for the synthesis of biologically active molecules. Its versatility in asymmetric synthesis allows for the development of enantiomerically pure drugs, which is essential for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Agrochemical Industry:
(4R,5R)-4,5-Dicyclohexyl-2-ethyl-1,3,2-dioxaborolane also finds application in the agrochemical industry, where it serves as a building block for the synthesis of various agrochemicals, such as pesticides and herbicides. Its unique reactivity and stereochemistry enable the development of novel and effective compounds for agricultural use.
Overall, (4R,5R)-4,5-Dicyclohexyl-2-ethyl-1,3,2-dioxaborolane is an important chemical in organic chemistry with diverse applications in research and industry, particularly in the fields of pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 152428-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,2 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 152428-72:
(8*1)+(7*5)+(6*2)+(5*4)+(4*2)+(3*8)+(2*7)+(1*2)=123
123 % 10 = 3
So 152428-72-3 is a valid CAS Registry Number.
152428-72-3Relevant academic research and scientific papers
Acyclic stereoselective boron alkylation reactions for the asymmetric synthesis of β-substituted α-amino acid derivatives
O'Donnell, Martin J.,Cooper, Jeremy T.,Mader, Mary M.
, p. 2370 - 2371 (2007/10/03)
Optically active syn- or anti-β-substituted-α-amino acid derivatives are prepared in 94 to ≥99% ee and 66-98% ds by reaction of the Schiff base acetate of glycine tert-butyl ester with chiral, nonracemic B-alkyl-9-BBN derivatives in the presence of the Cinchona alkaloid, cinchonidine (CdOH) or cinchonine (CnOH), base, and lithium chloride. Copyright
