717-75-9 Usage
Uses
Used in Pharmaceutical Industry:
3-acetyl-5-nitrobenzoic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into more complex molecular structures, contributing to the development of new drugs and medications.
Used in Organic Synthesis:
3-acetyl-5-nitrobenzoic acid is used as a building block in organic synthesis for its capacity to form more complex molecules, which can be further utilized in the creation of various organic compounds.
Used in Research and Development:
3-acetyl-5-nitrobenzoic acid is used in research and development as a chemical compound with unique properties and potential applications, allowing scientists and researchers to explore its capabilities and integrate it into innovative solutions across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 717-75-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 717-75:
(5*7)+(4*1)+(3*7)+(2*7)+(1*5)=79
79 % 10 = 9
So 717-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO5/c1-5(11)6-2-7(9(12)13)4-8(3-6)10(14)15/h2-4H,1H3,(H,12,13)
717-75-9Relevant academic research and scientific papers
Nitrogen-containing heterocycle derivatives, pharmaceutical compositions, and methods of use thereof as antiviral agents
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Page/Page column 34, (2010/11/28)
The present application provides nitrogen-containing heterocycle derivatives that are antiviral compounds that may be useful in the treatment of a viral infection. Compounds of Formula (I) and pharmaceutical compositions comprising a compound of Formula (I) may be administered to a subject for antiviral therapy or prophylaxis.
Process for the production of nitro derivatives of aromatic compounds
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, (2008/06/13)
Nitroderivates of aromatic compounds which are difficult to nitrate, can readily be obtained by nitration providing that the aromatic compound is treated with nitric acid or another nitrating agent in the presence of aliphatic or cycloaliphatic hydrocarbons monosubstituted or polysubstituted by halogen, the nitro group or an alkyl sulphonyl group, and the nitro derivative formed subsequently isolated.
