1134885-95-2

Basic information

• Product Name: 2H-1-Benzopyran-2-one, 6-fluoro-3,4-dihydro-4-phenyl-
• Synonyms: 2H-1-Benzopyran-2-one, 6-fluoro-3,4-dihydro-4-phenyl-;6-fluoro-3,4-dihydro-4-phenyl-2H-1-Benzopyran-2-one
• CAS NO: 1134885-95-2
• Molecular Formula: C₁₅H₁₁FO₂
• Molecular Weight: 242.2450432
• Mol File: 1134885-95-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 328.4±41.0 °C(Predicted)
• Appearance: /
• Density: 1.260±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2H-1-Benzopyran-2-one, 6-fluoro-3,4-dihydro-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1-Benzopyran-2-one, 6-fluoro-3,4-dihydro-4-phenyl-(1134885-95-2)
• EPA Substance Registry System: 2H-1-Benzopyran-2-one, 6-fluoro-3,4-dihydro-4-phenyl-(1134885-95-2)

Safety Data

• Hazardous Substances Data: 1134885-95-2(Hazardous Substances Data)

Usage

General Description

2H-1-Benzopyran-2-one, 6-fluoro-3,4-dihydro-4-phenyl- is a chemical compound with a molecular formula of C15H11FO2. It is a derivative of the compound 2H-1-benzopyran-2-one, and is characterized by the presence of a fluorine atom and a phenyl group in its structure. It is also known by the chemical name "6-fluoro-3,4-dihydro-4-phenylcoumarin" and has been studied for its potential use in medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals. Its chemical properties and structure make it a potentially important compound for further research and development in various fields of chemistry and biochemistry.

Upstream product

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Relevant articles and documents

Microwave accelerated the solvent-free synthesis of 4-aryl-3,4-dihydrocoumarin via the tandem reaction of cinnamic acids with phenols catalyzed by Amberlyst 15 resin

Amberlyst 15 resin supported the tandem reaction of cinnamic acids with phenols under solvent-free reaction condition has been introduced to afford 4-aryl-3,4-dihydrocoumarin (neoflavanone) derivatives. The efficiency of solid acidic sulfonic resin (A-15) has been illustrated in two reaction activation methods such as microwave irradiation and conventional heating. The important roles of Amberlyst 15 have been emphasized strongly through the high yields of 4-aryl-3,4-dihydrocoumarin in the shorter time under the assistance of microwave irradiation than of conventional heating, and its high recovery and reusability for six catalyst runs. The original catalyst as well as the recycled catalyst were characterized by XRD and FE-SEM to study the correlation of the surface of reused catalyst and its recyclability.