612-59-9 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Chloroquinoline is used as a raw material or intermediate in the synthesis of various pharmaceutical compounds. Its presence in the molecular structure can contribute to the development of new drugs with improved therapeutic properties.
Used in Agricultural Chemistry:
3-Chloroquinoline is used as a precursor in the production of agrochemicals, particularly those with antimicrobial properties. The chlorine atom on the quinoline structure provides bactericidal and fungicidal effects, making it a valuable component in the development of effective agricultural products.
Used in Antimicrobial Agents:
3-Chloroquinoline is used as an active ingredient in antimicrobial agents due to its potential bactericidal and fungicidal properties. Its presence in the molecular structure can enhance the effectiveness of these agents in controlling the growth of harmful microorganisms.
Used in Fluorescent Markers:
3-Chloroquinoline's intense fluorescence makes it a potential candidate for use in fluorescent markers. This property can be exploited in various applications, such as in the development of diagnostic tools or in the study of biological processes that require the visualization of specific molecules or cells.
Check Digit Verification of cas no
The CAS Registry Mumber 612-59-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 612-59:
(5*6)+(4*1)+(3*2)+(2*5)+(1*9)=59
59 % 10 = 9
So 612-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H6ClN/c10-8-5-7-3-1-2-4-9(7)11-6-8/h1-6H
612-59-9Relevant academic research and scientific papers
PHOTODECARBOXYLATIVE CHLORINATION OF CARBOXYLIC ACIDS VIA THEIR BENZOPHENONE OXIME ESTERS
Hasebe, Masato,Tsuchiya, Takashi
, p. 6287 - 6290 (2007/10/02)
Decarboxylative chlorination of various aromatic and aliphatic carboxylic acids is performed successfully by the photolysis of their benzophenone oxime esters in carbon tetrachloride and corresponding chloro compounds are prepared in good yields.High selective generation of the certain radical and efficiency of the stable radical precursor, benzophenone oxime ester, afford much advantage for radical chemistry.
