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Home  > 7-Fluoro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid

AA24749

1227465-79-3 | 7-Fluoro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $139.00 $97.00 -   +
1g 95% in stock $169.00 $118.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA24749
Chemical Name: 7-Fluoro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid
CAS Number: 1227465-79-3
Molecular Formula: C10H6FNO3
Molecular Weight: 207.1579
MDL Number: MFCD15527354
SMILES: Fc1ccc2c(c1)[nH]c(=O)cc2C(=O)O

 

Upstream Synthesis Route
  • 7-Fluoro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis processes. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its strong electron-withdrawing fluorine group provides unique reactivity, making it a valuable intermediate in organic synthesis.In chemical synthesis, $name$ plays a crucial role as a starting material for the preparation of quinoline-derived compounds. Its structural features allow for the introduction of diverse functional groups through a variety of synthetic transformations, such as nucleophilic substitutions, condensations, and cycloadditions.Additionally, the presence of a keto group in the molecule enables the synthesis of heterocyclic compounds with potential bioactivity. By judiciously modifying the chemical structure of $name$ through different synthetic routes, chemists can access a wide range of derivatives with tailored properties for specific applications in medicinal chemistry, materials science, and other fields.Overall, the strategic use of 7-Fluoro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid in chemical synthesis allows for the efficient and selective construction of complex molecules with desired functions, making it a valuable tool for researchers and practitioners in the field of organic chemistry.
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