20151-11-5 Usage
Uses
Used in Pharmaceutical Synthesis:
Quinoline, 2-chloro-4-(chloromethyl)is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of drug molecules with specific therapeutic properties, making it a valuable component in medicinal chemistry.
Used in Agrochemical Production:
Quinoline, 2-chloro-4-(chloromethyl)is also utilized in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals. Its presence in these products aids in enhancing crop protection and improving overall agricultural productivity.
Used in Research and Industrial Applications:
Quinoline, 2-chloro-4-(chloromethyl)plays a significant role in research and industrial applications, particularly in the field of organic chemistry. It serves as a versatile building block for the synthesis of various organic compounds and is used in the development of new chemical processes and methodologies.
Safety Precautions:
It is crucial to handle Quinoline, 2-chloro-4-(chloromethyl)with care, as it may pose hazards to human health and the environment if not properly managed. Adequate safety measures, such as wearing protective gear and following proper disposal procedures, should be implemented to minimize potential risks associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 20151-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,5 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20151-11:
(7*2)+(6*0)+(5*1)+(4*5)+(3*1)+(2*1)+(1*1)=45
45 % 10 = 5
So 20151-11-5 is a valid CAS Registry Number.
20151-11-5Relevant academic research and scientific papers
Kidwai, Mazaahir,Kohli, Seema,Kumar, Parven
, p. 586 - 587 (1998)
Rapid chlorination of side-chain Me groups of substituted quinolines and 2-mercapto-5-methyl 1,3,4-oxadiazole/ thiadiazole is reported using sodium Hypochlorits under microwave irradiation.
Synthesis and antiulcer activity of optical isomers of 2-(4-chlorobenzoylamino)-3-[2(1H)-quinolinon-4-yl]propionic acid (Rebamipide)
Otsubo,Morita,Uchida,Yamasaki,Kanbe,Shimizu
, p. 2906 - 2909 (2007/10/02)
The enantiomers of 2-(4-chlorobenzoylamino)-3-[2(1H)-quinolinon-4-yl]propionic acid [(±)-1, rebamipide, OPC-12759], a new antiulcer agent that enhances mucosal resistance, were synthesized from optically active α-amino acid derivatives of 2(1H)-quinolinone. The key intermediates, α-amino acid derivatives, were prepared by asymmetric synthesis and optical resolution. The (±)-1 was ahout 1.7 times as potent as the (-)-isomer in antiulcer activity against ethanol-induced gastric ulcers.
