913836-14-3 Usage
General Description
3-Chloro-5-methylphenylboronic acid is a chemical compound that belongs to the class of phenylboronic acids. It is a boronic acid derivative with a chloro and methyl group attached to the phenyl ring. 3-CHLORO-5-METHYLPHENYLBORONIC ACID is often used as a building block for the synthesis of various pharmaceuticals, agrochemicals, and organic materials. It is known for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an important reagent in organic synthesis. 3-Chloro-5-methylphenylboronic acid is typically 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.
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 articles and documents
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.
