5-Chloro-4-hydroxyquinoline-3-carboxylic acid


Chemical Name: 5-Chloro-4-hydroxyquinoline-3-carboxylic acid
CAS Number: 860205-48-7
Product Number: AG01ECA0(AGN-PC-0WAHTF)
Synonyms:
MDL No:
Molecular Formula: C10H6ClNO3
Molecular Weight: 223.61254

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-Chloro-4-hydroxyquinoline-3-carboxylic acid is a versatile compound widely utilized in chemical synthesis for its unique properties and diverse applications. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals due to its functional groups and reactivity.In chemical synthesis, 5-Chloro-4-hydroxyquinoline-3-carboxylic acid can be used as a precursor in the preparation of quinoline derivatives, which have shown promising biological activities such as antimicrobial, antimalarial, and anticancer properties. Its carboxylic acid group enables facile derivatization, leading to the synthesis of novel compounds with desired properties for drug discovery and development.Furthermore, the chloro and hydroxy groups on the quinoline ring offer opportunities for diverse chemical transformations, including halogenation, oxidation, and coupling reactions. These reactions enable the modification of the chemical structure of 5-Chloro-4-hydroxyquinoline-3-carboxylic acid to generate analogs and derivatives with enhanced biological activities or improved physicochemical properties.Overall, the application of 5-Chloro-4-hydroxyquinoline-3-carboxylic acid in chemical synthesis plays a crucial role in the development of new compounds for pharmaceutical, agricultural, and industrial purposes, showcasing its significance in modern organic chemistry research and innovation.