243140-14-9 Usage
Uses
Used in Pharmaceutical Research:
2-(2-METHYL-1,3-DIOXOLAN-2-YL)PHENYLBORONIC ACID is used as a building block for the synthesis of biologically active compounds, specifically in the development of potential drug candidates. Its ability to form C-C and C-N bonds through Suzuki-Miyaura coupling reactions makes it valuable in the production of complex organic molecules that can be further utilized in medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(2-METHYL-1,3-DIOXOLAN-2-YL)PHENYLBORONIC ACID is used as a reagent to facilitate the formation of C-C and C-N bonds. This capability is essential for constructing complex organic molecules that are vital in various chemical processes and applications.
Used in Agrochemical Production:
2-(2-METHYL-1,3-DIOXOLAN-2-YL)PHENYLBORONIC ACID is used as an important reagent in the production of agrochemicals. Its role in creating complex organic molecules contributes to the development of effective and innovative agrochemical products.
Used in Materials Science:
In materials science, 2-(2-METHYL-1,3-DIOXOLAN-2-YL)PHENYLBORONIC ACID is employed as a reagent for the synthesis of materials with specific properties. Its ability to form bonds and contribute to the structure of these materials makes it a valuable component in the advancement of materials with applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 243140-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,1,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 243140-14:
(8*2)+(7*4)+(6*3)+(5*1)+(4*4)+(3*0)+(2*1)+(1*4)=89
89 % 10 = 9
So 243140-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BO4/c1-10(14-6-7-15-10)8-4-2-3-5-9(8)11(12)13/h2-5,12-13H,6-7H2,1H3
243140-14-9Relevant academic research and scientific papers
Murafuji, Toshihiro,Sugimoto, Kenji,Yanagimoto, Sachiko,Moriya, Tomokazu,Sugihara, Yoshikazu,Mikata, Yuji,Kato, Masako,Yano, Shigenobu
, p. 929 - 942 (2001)
2′-Diethylboryl-4″-dimethylaminochalcone (1) and the related compounds (4)-(7) bearing a dioxyboryl group in the 2′-position were synthesized, and the effect of the intramolecular boron-oxygen coordinate bond on the spectroscopic characteristics of 4″-dimethylaminochalcone chromophore was examined by comparison with 4″-dimethylaminochalcone (2) using UV/VIS and fluorescence spectra.
Structure and spectroscopic characteristics of 2'-diethylboryl-4''- dimethylaminochalcone bearing an intramolecular boron-oxygen coordinate bond
Murafuji,Sugihara,Moriya,Mikata,Yano
, p. 683 - 685 (2008/10/08)
How formation of an intramolecular coordinate bond affects the molecular structure was examined in the structural comparison of 2'-diethylboryl-4''- dimethylaminochalcone (1) and 2'-ethylenedioxyboryl-4''-dimethylaminochalcone (2) with chloro-{2-[(4-dimethylaminostyryl) carbonyl] phenyl} (4-methyl- phenyl)] bismuthane (3) and 4''-dimethylaminochalcone (4).
