53868-40-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-Chlorophenyl)malondialdehyde is used as a pharmaceutical intermediate for the synthesis of various drugs and compounds with potential therapeutic applications. Its unique structure and reactivity may contribute to the development of new drugs with improved efficacy and reduced side effects.
Used in Chemical Research:
2-(4-Chlorophenyl)malondialdehyde is used as a research compound in the study of oxidative stress and related pathological processes. Its reactivity and potential biological effects make it a valuable tool for understanding the mechanisms of oxidative stress and its role in various diseases.
Used in Material Science:
2-(4-Chlorophenyl)malondialdehyde may be used in the development of new materials with specific chemical and physical properties. Its unique structure and reactivity could be utilized to create novel materials with applications in various industries, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 53868-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,6 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53868-40:
(7*5)+(6*3)+(5*8)+(4*6)+(3*8)+(2*4)+(1*0)=149
149 % 10 = 9
So 53868-40-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O3/c1-13-10-4-2-8(3-5-10)9(6-11)7-12/h2-7,11H,1H3/b9-6+
53868-40-9Relevant academic research and scientific papers
A Synthesis of Hydroxylated Isoflavylium Salts and Their Reduction Products
Liepa, Andris J.
, p. 2647 - 2655 (2007/10/02)
Phloroglucinol reacts with arylmalondialdehydes in the presence of hydrochloric acid to form 5,7-dihydroxyisoflavylium salts.Reduction of these salts can be utilized to form isoflav-2-enes, isoflav-3-enes or isoflavans.
Electronic Effects of Aryl and Heteroaryl Groups on the Rate of Nucleophilic Displacement of Chlorine from 5-Heteroaryl(or Aryl)-2-chloropyrimidines by Piperidine
Allen, David W.,Buckland, David J.,Hutley, Barrie G.
, p. 463 - 467 (2007/10/02)
The kinetics of nucleophilic displacement of chlorine from a series of 2-chloro-5-heteroaryl(or aryl)pyrimidines by piperidine have been studied in order to assess the electronic effects of the 5-substituent.The observed order of reactivity is 5-(1-methyl
