CAS 64369-55-7
:7-(diethylamino)-4-hydroxy-2H-chromen-2-one
Description:
7-(Diethylamino)-4-hydroxy-2H-chromen-2-one, also known as a derivative of coumarin, is a synthetic organic compound characterized by its chromenone structure, which features a benzopyrone core. This compound typically exhibits a yellow to orange color, which is common among many coumarin derivatives. It possesses a hydroxyl group at the 4-position and a diethylamino group at the 7-position, contributing to its solubility in organic solvents and potential biological activity. The presence of the diethylamino group enhances its electron-donating properties, which can influence its reactivity and interaction with biological targets. This compound is often studied for its potential applications in pharmaceuticals, particularly for its antioxidant, anti-inflammatory, and antimicrobial properties. Additionally, it may serve as a fluorescent probe in various analytical applications due to its ability to absorb and emit light. As with many chemical substances, safety and handling precautions should be observed, as it may pose health risks if not managed properly.
Formula:C13H15NO3
InChI:InChI=1/C13H15NO3/c1-3-14(4-2)9-5-6-10-11(15)8-13(16)17-12(10)7-9/h5-8,15H,3-4H2,1-2H3
SMILES:CCN(CC)c1ccc2c(cc(=O)oc2c1)O
Synonyms:- 2H-1-benzopyran-2-one, 7-(diethylamino)-4-hydroxy-
- 4-Hydroxy-7-Diethiamino-Coumarine
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Found 4 products.
4-HYDROXY-7-DIETHIAMINO-COUMARINE
CAS:Formula:C13H15NO3Purity:97%Color and Shape:SolidMolecular weight:233.2677-Diethylamino-4-hydroxy-chromen-2-one
CAS:Controlled ProductFormula:C13H15NO3Color and Shape:NeatMolecular weight:233.2637-Diethylamino-4-hydroxy-chromen-2-one
CAS:<p>7-Diethylamino-4-hydroxy-chromen-2-one is a fluorescent chemical compound that belongs to the family of atypical fluorophores. It has a number of photophysical properties, including fluorescence and regression, which are characteristic of amines. 7-Diethylamino-4-hydroxy-chromen-2-one can be synthesized from diazonium salt and 4-hydroxycoumarin. This chemical compound has been used as a fluorescent probe for nucleophilic reactions in various types of organic molecules. The nature of this fluorophore is unknown, but it may be due to its ability to shift the wavelength of fluorescence by up to 400 nm.</p>Formula:C13H15NO3Purity:Min. 95%Molecular weight:233.26 g/mol



