23858-59-5 Usage
General Description
3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxamide is a chemical compound with the molecular formula C10H8Cl2N2O2. It is a derivative of isoxazole and belongs to the class of amides. 3-(2,6-DICHLOROPHENYL)-5-METHYLISOXAZOLE-4-CARBOXAMIDE is used in medicinal chemistry as a building block for designing and synthesizing new pharmaceutical compounds. Its chemical structure and properties make it suitable for various biological activities, such as anti-inflammatory and antibacterial effects. Its potential applications in drug development and research make it an important compound in the field of chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 23858-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,5 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23858-59:
(7*2)+(6*3)+(5*8)+(4*5)+(3*8)+(2*5)+(1*9)=135
135 % 10 = 5
So 23858-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H8Cl2N2O2/c1-5-8(11(14)16)10(15-17-5)9-6(12)3-2-4-7(9)13/h2-4H,1H3,(H2,14,16)
23858-59-5Relevant articles and documents
New Derivatives of Asymmetic Chloral Aminals.
Barczynski,Eckstein
, p. 176 - 177 (2007/10/09)
This paper is concerned by newly developed fungicides. In the reported research program, first there were prepared parent carboxylic acids of benodanil, mebenil, furcarbanil, pyracarbolid, carboxin and G-696. Then they were transformed into respective amides. From the latter, by action of chloral, its semiaminals were obtained. Under analogous conditions, for the purpose of comparison in future tests on biological activity, chloral semiaminals were prepared from amides of the following acids: phenylthio - and phenylsulfoacetic, 3-(2 prime -chlorophenyl) - and 3-(2 prime ,6 prime -dichlorophenyl) - 5 -methylisoxazolcarboxylic-4. By action of phenyl isocyanate, 4-chlorophenyl and 3,4-dichlorophenyl on all chloral semiaminals synthesized respective asymmetric aminals of this aldehyde were obtained. The above reactions run with carbon dioxide elimination and give high yields of products.
