883899-03-4 Usage
Uses
Used in Organic Synthesis:
2-Cyano-3-(trifluoromethyl)phenyl boronic acid neopentyl glycol ester is used as a reagent or intermediate in the production of various pharmaceuticals, agrochemicals, and materials. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Research and Development:
2-CYANO-3-(TRIFLUOROMETHYL)PHENYL BORONIC ACID NEOPENTYL GLYCOL ESTER is also utilized in the development of new chemical compounds and for research purposes in the field of organic and medicinal chemistry. Its versatility and reactivity make it an important tool for scientists working on the design and synthesis of novel molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 883899-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,8,9 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 883899-03:
(8*8)+(7*8)+(6*3)+(5*8)+(4*9)+(3*9)+(2*0)+(1*3)=244
244 % 10 = 4
So 883899-03-4 is a valid CAS Registry Number.
883899-03-4Relevant academic research and scientific papers
Novel syntheses of fluorenones via nitrile-directed palladium-catalyzed C-H and dual C-H bond activation
Wan, Jung-Chih,Huang, Jun-Min,Jhan, Yu-Huei,Hsieh, Jen-Chieh
supporting information, p. 2742 - 2745 (2013/07/19)
Novel procedures for the [Pd]/[Ag]/TFA system catalyzed cascade reactions of nitrile directed remote C-H and dual C-H bond activation with insertion of nitrile were developed, which afforded variously polysubstituted fluorenones in moderate to good yields with tolerance of a wide variety of substrates.
Synthesis of substituted 2-cyanoarylboronic esters
Lysen, Morten,Hansen, Henriette M.,Begtrup, Mikael,Kristensen, Jesper L.
, p. 2518 - 2520 (2007/10/03)
The synthesis of substituted 2-cyanoarylboronic esters is described via lithiation/in situ trapping of the corresponding methoxy-, trifluoromethyl-, fluoro-, chloro-, and bromobenzonitriles. The crude arylboronic esters were obtained in high yields and pu
