372193-68-5 Usage
Uses
Used in Organic Synthesis:
[2-(E-3-Methoxy-3-oxo-1-propen-1-yl)phenyl]boronic acid is used as a reagent in the Suzuki-Miyaura coupling reaction for creating carbon-carbon bonds. This reaction is a widely utilized method in organic synthesis, allowing for the formation of new chemical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [2-(E-3-Methoxy-3-oxo-1-propen-1-yl)phenyl]boronic acid is used as a potential building block for drug discovery. Its unique structure and reactivity make it a valuable component in the development of new pharmaceutical agents.
Used in the Synthesis of Complex Molecules:
MOPPA is also utilized in the synthesis of complex molecules, where its boronic acid functional group can be employed to form various types of chemical bonds and contribute to the overall structure and properties of the target molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 372193-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,1,9 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 372193-68:
(8*3)+(7*7)+(6*2)+(5*1)+(4*9)+(3*3)+(2*6)+(1*8)=155
155 % 10 = 5
So 372193-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BO4/c1-15-10(12)7-6-8-4-2-3-5-9(8)11(13)14/h2-7,13-14H,1H3/b7-6+
372193-68-5Relevant academic research and scientific papers
Bromo-boronolactonization of olefins
Falck,Bondlela,Venkataraman,Srinivas
, p. 7148 - 7150 (2007/10/03)
Exposure of a variety of mono- and disubstituted ortho-alkenylarylboronic acids to NBS in THF/H2O under neutral conditions affords bromo-boronolactones, in some instances, with exceptional regiocontrol. The adducts, analogous to those formed by carboxylic acids, are shown to be useful synthetic intermediates.