871333-97-0 Usage
Uses
Used in Organic Synthesis:
4,4-DIMETHYLCYCLOHEXA-1,5-DIENYLBORONIC ACID PINACOL ESTER is used as a cross-coupling reagent for the formation of carbon-carbon bonds, facilitating the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 4,4-DIMETHYLCYCLOHEXA-1,5-DIENYLBORONIC ACID PINACOL ESTER is used as a building block in the preparation of pharmaceuticals, contributing to the modulation of biological activities and properties of target compounds for therapeutic applications.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, 4,4-DIMETHYLCYCLOHEXA-1,5-DIENYLBORONIC ACID PINACOL ESTER is utilized as a key component in the synthesis of agrochemicals, enhancing the effectiveness and selectivity of these compounds in agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 871333-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,3,3 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 871333-97:
(8*8)+(7*7)+(6*1)+(5*3)+(4*3)+(3*3)+(2*9)+(1*7)=180
180 % 10 = 0
So 871333-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H23BO2/c1-12(2)9-7-11(8-10-12)15-16-13(3,4)14(5,6)17-15/h7-9H,10H2,1-6H3
871333-97-0Relevant academic research and scientific papers
Chang, Taiwei,Huo, Jingfeng,Lei, Ming,Ping, Yifan,Wang, Jianbo,Wang, Qianyue,Wang, Rui
, p. 9769 - 9780 (2021)
The palladium-catalyzed oxidative borylation reaction of N-tosylhydrazones has been developed. The reaction features mild conditions, broad substrate scope, and good functional group tolerance. It thus represents a highly efficient and practical method for the synthesis of di-, tri-, and tetrasubstituted alkenylboronates from readily available N-tosylhydrazones. One-pot Suzuki coupling and other transformations highlight the synthetic utility of the approach. DFT calculations have revealed that palladium-carbene formation and subsequent boryl migratory insertion are the key steps in the catalytic cycle. The high stereoselectivity observed in the formation of trisubstituted alkenylboronates has been explained by distortion-interaction analysis and NBO analysis.
