1028-71-3

Usage

Uses

Used in Pharmaceutical Applications:
(8-hydroxyquinolin-5-yl)(phenyl)methanone is used as a component in the development of metal-binding drugs, leveraging its strong metal chelation properties for potential pharmaceutical formulations.
Used in Organic Synthesis:
(8-hydroxyquinolin-5-yl)(phenyl)methanone serves as a building block in organic synthesis, contributing to the construction of more complex molecules for various applications.
Used in Research and Development:
(8-hydroxyquinolin-5-yl)(phenyl)methanone is also utilized in research and development settings to further explore its properties and potential applications, as more investigation is required to fully understand its capabilities and uses across different industries.

Upstream product

• 148-24-3 8-quinolinol 
• 98-88-4 benzoyl chloride 
• 86-75-9 Benzoxiquine 

Downstream Products

• 102313-70-2 (8-hydroxy-7-piperidinomethyl-[5]quinolyl)-phenyl ketone 
• 103756-75-8 (7-{[ethyl-(2-diethylamino-ethyl)-amino]-methyl}-8-hydroxy-[5]quinolyl)-phenyl ketone 
• 94378-26-4 (7-dimethylaminomethyl-8-hydroxy-[5]quinolyl)-phenyl ketone 
• 6954-93-4 5-benzylquinolin-8-ol 
• 78586-18-2 bis(5-benzoyl-8-quinolinolato)dibutyltin(IV) 
• 78586-21-7 bis(5-benzoyl-8-quinolinolato)diphenyltin(IV) 
• 78586-27-3 Cl₂Sn((C₆H₅CO)C₉H₅NO)2 

Relevant academic research and scientific papers

1, 2, 3-TRIAZOLE CONTAINING PROTEIN KINASE SENSORS

The present invention generally relates to compositions and methods for determining kinase activity. In some cases, the compositions comprise a triazole heterocycle. In some embodiments, the compositions comprise a quinoline moiety. In one aspect, the pre

1,2,3,4-tetrahydro-8-quinolinol derivatives and anti-allergic use thereof

Leukotriene biosynthesis in macrophage cells is inhibited by compounds having the formula STR1 and pharmaceutically acceptable salts thereof, wherein R1 and R2 are each hydrogen and R3 is alkyl or arylalkyl; R1

Photo-Fries Rearrangement: Rearrangement of Benzoyloxy Compounds

Photo-Fries migration of the benzoyl group in 1-benzoyloxy-5-methoxy naphthalene, 1,4-dibenzoyloxy-2-methyl naphthalene, 1,4-dibenzoyloxy naphthalene, 1,5-dibenzoyloxy naphthalene, 8-benzoyloxy quinoline, 1,2-dibenzoyloxy benzene, 1,3-dibenzoyloxy benzene, and 1,4-dibenzoyloxy benzene afforded the corresponding mono and di-C-benzoyl products. - Keywords: Naphthyl benzoate derivatives; 8-Benzoyloxy quinoline; Phenyl dibenzoates