32608-29-0 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Dichloro-8-methoxyquinoline is used as an active pharmaceutical ingredient for its antimicrobial properties, making it suitable for the development of drugs to treat bacterial infections.
Used in Veterinary Medicine:
In the veterinary field, 2,4-Dichloro-8-methoxyquinoline is used as a component in veterinary drugs to combat microbial infections in animals, ensuring their health and well-being.
Used in Organic Synthesis:
2,4-Dichloro-8-methoxyquinoline serves as a building block in the synthesis of other organic compounds, contributing to the development of new chemical entities with potential applications in various industries.
Safety Precautions:
Due to its potential health hazards, 2,4-Dichloro-8-methoxyquinoline should be handled with care and used in accordance with established safety guidelines to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 32608-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,6,0 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32608-29:
(7*3)+(6*2)+(5*6)+(4*0)+(3*8)+(2*2)+(1*9)=100
100 % 10 = 0
So 32608-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H7Cl2NO/c1-14-8-4-2-3-6-7(11)5-9(12)13-10(6)8/h2-5H,1H3
32608-29-0Relevant academic research and scientific papers
Synthesis of 6-methoxy-N 2,N 2,N 4,N 4,N 5,N 5-hexamethylquinoline-2,4,5-triamine - A new representative of quinoline proton sponges
Dyablo, Olga V.,Pozharskii, Alexander F.,Shmoilova, Elena A.,Savchenko, Aleksey O.
, p. 250 - 258 (2016/01/12)
[Figure not available: see fulltext.] We report the synthesis of 4-chloro-2-methyl-5-nitro- and 2,4-dichloro-5-nitroquinolines, containing methoxy groups at positions 6 and 8. The reaction of these compounds with dimethylamine solution in alcohol was shown to produce not only aminodehalogenation products, but also resulted in nucleophilic substitution of the methoxy groups. The reduction of 6-methoxy-N 2,N 2,N 4,N 4-tetramethyl-5-nitroquinoline-2,4-diamine with subsequent methylation gave 6-methoxy-N 2,N 2,N 4,N 4,N 5,N 5-hexamethylquinoline-2,4,5-triamine, a new representative of quinoline proton sponges.
