196803-72-2 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Chloro-6,8-dimethylquinoline is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
4-CHLORO-6,8-DIMETHYLQUINOLINE is also employed in the synthesis of agrochemicals, playing a role in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used in Antimalarial Applications:
4-Chloro-6,8-dimethylquinoline has been studied for its potential antimalarial properties, indicating its use as a precursor in the development of treatments for malaria.
Used in Anti-inflammatory Applications:
4-CHLORO-6,8-DIMETHYLQUINOLINE has shown promise in anti-inflammatory research, suggesting its use in the formulation of medications aimed at reducing inflammation and related symptoms.
Used in Organic Compound Preparation:
As a building block, 4-chloro-6,8-dimethylquinoline is used in the preparation of other organic compounds, expanding its utility in various chemical reactions and syntheses.
Used in Materials Science:
4-Chloro-6,8-dimethylquinoline may have applications in the field of materials science, potentially contributing to the development of new materials with specific properties for various industries.
Used as a Chemical Research Reagent:
4-CHLORO-6,8-DIMETHYLQUINOLINE serves as a reagent in chemical research, aiding in experiments and studies to advance scientific understanding and innovation in chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 196803-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,8,0 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 196803-72:
(8*1)+(7*9)+(6*6)+(5*8)+(4*0)+(3*3)+(2*7)+(1*2)=172
172 % 10 = 2
So 196803-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClN/c1-7-5-8(2)11-9(6-7)10(12)3-4-13-11/h3-6H,1-2H3
196803-72-2Relevant academic research and scientific papers
Synthesis and structural investigation of an oxazinoquinolinespirohexadienone that only exists as its long-wavelength ring-opened quinonimine isomer
Pollock, Benjamin J.,Sikes, Christos A.,Ter Louw, Ryan P.,Hawken, Scott R.,Speelman, Amy L.,Lynch, Eugene J.,Gillmore, Jason G.,Stanford, Daniel J.,Wheeler, Kraig A.
, p. 8689 - 8695,7 (2020/09/15)
The spirocyclic oxazinoquinolinespirohexadienone (OSHD) photochromes are computationally predicted to be an attractive target as electron deficient analogues of the perimidinespirohexadienone (PSHD) photochromes, for eventual application as photochromic photooxidants. We have found the literature method for their preparation unsuitable and present an alternative synthesis. Unfortunately the product of this synthesis is the long wavelength (LW) ring-opened quinonimine isomer of the OSHD. We have found this isomer does not close to the spirocyclic short wavelength isomer (SW) upon prolonged standing in the dark, unlike other PSHD photochromes. The structure of this long wavelength isomer was found by NMR and X-ray crystallography to be exclusively the quinolinone (keto) tautomer, though experimental cyclic voltammetry supported by our computational methodology indicates that the quinolinol (enol) tautomer (not detected by other means) may be accessible through a fast equilibrium lying far toward the keto tautomer. Computations also support the relative stability order of keto LW over enol LW over SW.
