73863-49-7 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-3-(chloromethyl)-7-methoxyquinoline is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms. Its antifungal and antimicrobial properties make it a promising candidate for the development of new antibiotics and antifungal drugs.
Used in Agricultural Industry:
Due to its capability to inhibit the growth of microorganisms, 2-chloro-3-(chloromethyl)-7-methoxyquinoline may also be utilized as a pesticide or antiparasitic agent, offering potential applications in protecting crops and managing pests.
Used in Research and Development:
The chemical structure and properties of 2-chloro-3-(chloromethyl)-7-methoxyquinoline make it a valuable compound for further research and development, particularly in exploring its potential applications in pharmaceuticals and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 73863-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,6 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73863-49:
(7*7)+(6*3)+(5*8)+(4*6)+(3*3)+(2*4)+(1*9)=157
157 % 10 = 7
So 73863-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H9Cl2NO/c1-15-9-3-2-7-4-8(6-12)11(13)14-10(7)5-9/h2-5H,6H2,1H3
73863-49-7Relevant academic research and scientific papers
A Versatile New Synthesis of Quinolines and Related Fused Pyridines. Part 8. Conversion of Anilides into 3-Substituted Quinolines and into Quinoxalines
Meth-Cohn, Otto,Rhouati, Salah,Tarnowski, Brian,Robinson, Andrew
, p. 1537 - 1543 (2007/10/02)
Anilides (4) (ArNHCOCH2R) are readily converted into 2-chloro-3-R-quinolines (5) under Vilsmeier conditions and the 3-chloro-group may be removed with zinc and acetic acid yielding 3-substituted quinolines (7).When N-nitrosodialkylamines are used in place of dimethylformamide as the Vilsmeier agent, the anilides are converted into 2-chloroquinoxalines in low yields.Several by-products are formed and the mechanisms have been explored.Thus, the formation of ethyl N-arylcarbamate from the corresponding propionanilide is shown to involve an C->O alkyl migration related to a Wolff rearrangement, while N-arylformimidoyl dichloride (18), nitriles, and isocyanides are derived from C-C cleavage of the substituted side-chain.Variation of the acid chloride component of the Vilsmeier reagent or of the solvent was generally unproductive though use of phosphoryl bromide instead of the chloride caused conversion of anilides into bromoquinolines in low yields.
