81892-46-8 Usage
Uses
Used in Pharmaceutical Industry:
(4Z)-6-fluoro-1-propanoyl-2,3-dihydroquinolin-4(1H)-one oxime is used as a potential therapeutic agent for its possible antimicrobial, antiviral, or anti-inflammatory properties. (4Z)-6-fluoro-1-propanoyl-2,3-dihydroquinolin-4(1H)-one oxime's specific applications within the pharmaceutical industry may vary depending on the results of ongoing research and development.
Used in Research and Development:
In the field of scientific research, (4Z)-6-fluoro-1-propanoyl-2,3-dihydroquinolin-4(1H)-one oxime serves as a valuable compound for exploring its potential biological and pharmacological activities. Its use in research can contribute to the advancement of knowledge in various areas, including drug discovery, medicinal chemistry, and the development of novel therapeutic strategies.
Used in Chemical Synthesis:
(4Z)-6-fluoro-1-propanoyl-2,3-dihydroquinolin-4(1H)-one oxime may also be utilized as a key intermediate or building block in the synthesis of more complex molecules with potential applications in various industries, such as pharmaceuticals, agrochemicals, or materials science. Its unique structure and functional groups make it a promising candidate for further chemical modifications and exploration.
Check Digit Verification of cas no
The CAS Registry Mumber 81892-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,9 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81892-46:
(7*8)+(6*1)+(5*8)+(4*9)+(3*2)+(2*4)+(1*6)=158
158 % 10 = 8
So 81892-46-8 is a valid CAS Registry Number.
81892-46-8Relevant academic research and scientific papers
4-Oximino-1,2,3,4-tetrahydroquinoline derivatives
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, (2008/06/13)
4-oximino-1,2,3,4-tetrahydroquinoline derivatives of the formula (I): STR1 wherein X represents a halogen atom and Y represents a hydrogen atom, a straight-chain or branched-chain alkyl group, a halogen-substituted lower alkyl group, a phenylalkyl group, a phenylalkenyl group, an unsubstituted or halogen-substituted phenyl group, a nitrogen-containing aromatic group, a straight-chain or branched-chain alkoxy group or an alkyl-substituted or phenyl-substituted amino group.
