CAS 1786-05-6
:4-Hydroxy-3-phenylcoumarin
Description:
4-Hydroxy-3-phenylcoumarin, with the CAS number 1786-05-6, is a chemical compound belonging to the coumarin family, characterized by its fused benzene and α-pyrone rings. This compound typically exhibits a pale yellow to white crystalline appearance. It is known for its potential biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties, making it of interest in pharmaceutical and cosmetic applications. The presence of the hydroxyl group at the 4-position and the phenyl group at the 3-position contributes to its unique reactivity and solubility characteristics. 4-Hydroxy-3-phenylcoumarin can undergo various chemical reactions, such as esterification and oxidation, which can modify its properties and enhance its utility in different formulations. Additionally, it may exhibit fluorescence, which can be advantageous in analytical applications. As with many organic compounds, its stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 4-Hydroxy-3-phenylcoumarin is a versatile compound with significant potential in various fields of research and industry.
Formula:C15H10O3
InChI:InChI=1S/C15H10O3/c16-14-11-8-4-5-9-12(11)18-15(17)13(14)10-6-2-1-3-7-10/h1-9,16H
InChI key:InChIKey=CBHMYFPBBDCWSY-UHFFFAOYSA-N
SMILES:OC1=C(C(=O)OC=2C1=CC=CC2)C3=CC=CC=C3
Synonyms:- 2-hydroxy-3-phenyl-4H-chromen-4-one
- 2H-1-Benzopyran-2-one, 4-hydroxy-3-phenyl-
- 3-Phenyl-4-hydroxycoumarin
- 4-Hydroxy-3-Phenyl-2H-1-Benzopyran-2-On
- 4-Hydroxy-3-Phenyl-2H-1-Benzopyran-2-One
- 4-Hydroxy-3-Phenyl-Coumari
- Aurora Ka-3168
- Coumarin, 4-hydroxy-3-phenyl-
- Hydroxy-3-Phenylcoumarin, 4-
- NSC 251152
- 4-Hydroxy-3-phenylcoumarin
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Found 3 products.
4-Hydroxy-3-phenyl-2H-chromen-2-one
CAS:Formula:C15H10O3Purity:95%Color and Shape:SolidMolecular weight:238.23814-Hydroxy-3-phenylcoumarin
CAS:<p>4-Hydroxy-3-phenylcoumarin is an organic compound, which is a derivative of coumarin. It is synthetically derived through chemical modification processes that introduce a hydroxy group and a phenyl ring to the coumarin core structure. Its mechanism of action involves the inhibition of vitamin K epoxide reductase, an enzyme critical for the cyclic conversion of vitamin K. This inhibition prevents the activation of vitamin K-dependent clotting factors, thereby exerting its anticoagulant effects.</p>Formula:C15H10O3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:238.24 g/mol


