3-Hydroxy-6-methoxy-2-phenyl-1H-quinolin-4-one

≥95%

Reagent Code: #196147
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CAS Number 60343-76-2

science Other reagents with same CAS 60343-76-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.28 g/mol
Formula C₁₆H₁₃NO₃
thermostat Physical Properties
Boiling Point 459.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.315±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of flavonoids and other bioactive heterocyclic compounds. Exhibits strong antioxidant properties, making it valuable in pharmaceutical research for developing drugs targeting oxidative stress-related diseases. Shows potential in anticancer studies due to its ability to inhibit specific tumor cell growth. Also employed in the development of fluorescent probes for sensing metal ions in environmental and biological systems. Its structural features allow for easy modification, enhancing its utility in medicinal chemistry and drug design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿42,640.00
1mg
10-20 days ฿14,240.00
3-Hydroxy-6-methoxy-2-phenyl-1H-quinolin-4-one
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Used as a key intermediate in the synthesis of flavonoids and other bioactive heterocyclic compounds. Exhibits strong antioxidant properties, making it valuable in pharmaceutical research for developing drugs targeting oxidative stress-related diseases. Shows potential in anticancer studies due to its ability to inhibit specific tumor cell growth. Also employed in the development of fluorescent probes for sensing metal ions in environmental and biological systems. Its structural features allow for easy m

Used as a key intermediate in the synthesis of flavonoids and other bioactive heterocyclic compounds. Exhibits strong antioxidant properties, making it valuable in pharmaceutical research for developing drugs targeting oxidative stress-related diseases. Shows potential in anticancer studies due to its ability to inhibit specific tumor cell growth. Also employed in the development of fluorescent probes for sensing metal ions in environmental and biological systems. Its structural features allow for easy modification, enhancing its utility in medicinal chemistry and drug design.

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