372193-52-7 Usage
Functional Groups
Boronic acid (-B(OH)2), alkene (C=C)
Configuration
Z-configuration of the double bond
Structure
Consists of a benzene ring attached to a seven-carbon chain with a double bond in the Z-configuration.
Application
Used as a reagent in organic synthesis, particularly in palladium-catalyzed coupling reactions for forming carbon-carbon bonds.
Interest in pharmaceutical development and materials synthesis.
Research Focus
Investigation for potential applications in sensor technology.
Studied for its role in medical diagnostic tool development.
Check Digit Verification of cas no
The CAS Registry Mumber 372193-52-7 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, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 372193-52:
(8*3)+(7*7)+(6*2)+(5*1)+(4*9)+(3*3)+(2*5)+(1*2)=147
147 % 10 = 7
So 372193-52-7 is a valid CAS Registry Number.
372193-52-7Relevant 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.
