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580-20-1

quinolin-7-ol

Catalog#: AR003O4Q  |   CAS#: 580-20-1  |   MDL#: MFCD00016730  |   MF: C9H7NO  |   MW: 145.158

Packsize Purity Price Availability Quantity
1g 98% $5.00 Global Stock Buy Now Add To Cart
5g 98% $12.00 Global Stock Buy Now Add To Cart
10g 98% $23.00 Global Stock Buy Now Add To Cart
25g 98% $56.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003O4Q
Chemical Name quinolin-7-ol
CAS Number 580-20-1
Molecular Formula C9H7NO
Molecular Weight 145.158
MDL Number MFCD00016730
SMILES Oc1ccc2c(c1)nccc2
NSC Number 87630

Quinolin-7-ol, also known as 7-hydroxyquinoline, is a versatile compound widely utilized in chemical synthesis processes. This organic compound plays a crucial role in various reactions and applications due to its unique structure and properties. In chemical synthesis, Quinolin-7-ol is commonly employed as a chelating agent, facilitating the formation of stable complexes with metal ions. This capability makes it valuable in coordination chemistry and metal-catalyzed reactions.One of the key applications of Quinolin-7-ol is its use as a ligand in transition metal catalysis. By forming metal complexes with transition metals such as palladium, ruthenium, or nickel, Quinolin-7-ol can enhance the selectivity and efficiency of various chemical transformations. This includes processes like cross-coupling reactions, C-H activation, and asymmetric catalysis, where the coordination chemistry of Quinolin-7-ol significantly influences the reactivity and outcome of the reaction.Furthermore, Quinolin-7-ol serves as a precursor in the synthesis of bioactive molecules and pharmaceutical intermediates. Its functional groups enable derivatization for the preparation of diverse compounds with potential pharmacological activities. By incorporating Quinolin-7-ol into molecular structures, chemists can access new chemical entities with tailored properties for drug discovery and development.In summary, Quinolin-7-ol plays a pivotal role in chemical synthesis, particularly in metal-catalyzed reactions and pharmaceutical chemistry. Its ability to coordinate with metal ions and participate in diverse transformations makes it a valuable tool for synthetic chemists seeking to achieve specific molecular designs and functional group transformations.
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