913836-14-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-5-methylphenylboronic acid is used as a building block for the synthesis of various pharmaceuticals due to its ability to participate in Suzuki-Miyaura cross-coupling reactions, which is crucial for the production of biologically active molecules.
Used in Agrochemical Industry:
3-Chloro-5-methylphenylboronic acid is used as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective and targeted pest control agents.
Used in Organic Material Synthesis:
3-Chloro-5-methylphenylboronic acid is used as a reagent in the synthesis of various organic materials, taking advantage of its ability to form stable intermediates and participate in cross-coupling reactions, which is essential for creating new materials with desired properties.
Used in Medicinal Chemistry and Drug Discovery:
3-Chloro-5-methylphenylboronic acid is used as a key intermediate in the production of various biologically active molecules, making it an important compound in the field of medicinal chemistry and drug discovery, where it aids in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 913836-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,8,3 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 913836-14:
(8*9)+(7*1)+(6*3)+(5*8)+(4*3)+(3*6)+(2*1)+(1*4)=173
173 % 10 = 3
So 913836-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BClO2/c1-5-2-6(8(10)11)4-7(9)3-5/h2-4,10-11H,1H3
913836-14-3Relevant academic research and scientific papers
One-pot synthesis of arylboronic acids and aryl trifluoroborates by Ir-catalyzed borylation of arenes
Murphy, Jaclyn M.,Tzschucke, C. Christoph,Hartwig, John F.
, p. 757 - 760 (2007/10/03)
(Chemical Equation Presented) The synthesis of arylboronic acids and aryl trifluoroborates in a one-pot sequence by Ir-calalyzed borylation of arenes is reported. To prepare the arylboronic acids, the Ir-catalyzed borylation is followed by oxidative cleavage of the boronic ester with NaIO4. To prepare the aryltrifluoroborate, the Ir-catalyzed borylation is followed by displacement of pinacol by KHF2. These two-step sequences give products that are more reactive toward subsequent chemistry than the initially formed pinacol boronates.
