73863-50-0 Usage
Description
2-Chloro-3-(2-chloroethyl)-7-methylquinoline is a heterocyclic aromatic compound with the chemical formula C13H11Cl2N. It is a derivative of quinoline, featuring two chlorine atoms, one ethyl group, and one methyl group attached to the quinoline ring. 2-Chloro-3-(2-chloroethyl)-7-methylquinoline may exhibit potential biological activity, making it a valuable compound for pharmaceutical and chemical research, as well as for further study in organic chemistry and drug development.
Uses
Used in Pharmaceutical Research:
2-Chloro-3-(2-chloroethyl)-7-methylquinoline is used as a compound with potential biological activity for the development of new pharmaceuticals. Its unique structure and functional groups may contribute to its interaction with biological targets, offering opportunities for the treatment of various diseases.
Used in Chemical Research:
In the field of chemical research, 2-Chloro-3-(2-chloroethyl)-7-methylquinoline is used as a valuable compound for studying its synthesis and properties. Understanding its reactivity and behavior in chemical reactions can provide insights into the development of new synthetic routes and applications in organic chemistry.
Used in Drug Development:
2-Chloro-3-(2-chloroethyl)-7-methylquinoline is utilized in drug development as a potential lead compound. Its unique structure and potential biological activity make it a promising candidate for further optimization and development into effective therapeutic agents.
Used in Organic Chemistry:
In the realm of organic chemistry, 2-Chloro-3-(2-chloroethyl)-7-methylquinoline serves as a subject for exploring new synthetic methods and reaction mechanisms. Its synthesis and properties can contribute to the advancement of organic chemistry techniques and the discovery of novel compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 73863-50-0 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, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73863-50:
(7*7)+(6*3)+(5*8)+(4*6)+(3*3)+(2*5)+(1*0)=150
150 % 10 = 0
So 73863-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H11Cl2N/c1-8-2-3-9-7-10(4-5-13)12(14)15-11(9)6-8/h2-3,6-7H,4-5H2,1H3
73863-50-0Relevant articles and documents
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.
