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62542-44-3

1-methyl-2-oxo-1,2-dihydroquinoline-4-carboxylic acid

Catalog#: AR00EEJO  |   CAS#: 62542-44-3  |   MDL#: MFCD03197124  |   MF: C11H9NO3  |   MW: 203.1941

Packsize Purity Price Availability Quantity
100mg 95% $27.00 Global Stock Buy Now Add To Cart
250mg 95% $46.00 Global Stock Buy Now Add To Cart
1g 95% $113.00 Global Stock Buy Now Add To Cart
5g 95% $503.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EEJO
Chemical Name 1-methyl-2-oxo-1,2-dihydroquinoline-4-carboxylic acid
CAS Number 62542-44-3
Molecular Formula C11H9NO3
Molecular Weight 203.1941
MDL Number MFCD03197124
SMILES OC(=O)c1cc(=O)n(c2c1cccc2)C

1-Methyl-2-oxo-1,2-dihydroquinoline-4-carboxylic acid, often referred to as $name$, serves a pivotal role in chemical synthesis as a versatile building block. Its unique structure and functional groups make it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, $name$ can undergo a range of reactions to introduce different substituents or modify its core structure. For instance, its carboxylic acid group can participate in esterification or amidation reactions to form esters or amides, respectively. Furthermore, the quinoline ring system offers opportunities for further diversification through functionalization of the nitrogen atom or the aromatic ring.The presence of the carbonyl group in $name$ makes it a suitable substrate for a variety of reactions, including nucleophilic addition, acylation, or condensation reactions. By judiciously choosing reaction conditions and reagents, chemists can precisely manipulate the molecular structure of $name$ to yield complex molecules with desired properties.Overall, the strategic placement of functional groups in 1-Methyl-2-oxo-1,2-dihydroquinoline-4-carboxylic acid makes it a valuable and versatile tool in the hands of synthetic chemists, enabling the efficient construction of diverse compounds for various applications.
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