2-Propen-1-one, 1,3-bis(4-fluorophenyl)-3-hydroxy-

95%

Reagent Code: #223322
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CAS Number 62375-96-6

science Other reagents with same CAS 62375-96-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.2355 g/mol
Formula C₁₅H₁₀F₂O₂
badge Registry Numbers
MDL Number MFCD32693207
thermostat Physical Properties
Boiling Point 391.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.307±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory, antidiabetic, anticancer, and antimicrobial agents. The fluorine and hydroxyl groups in its structure enhance biological activity and support the formation of chalcone derivatives. It is also employed in research on smart materials and chemical sensors due to its responsiveness to environmental changes, such as light or pH. Commonly used in research settings to explore new therapeutic molecules and advanced materials owing to the reactivity of its carbonyl and hydroxyl groups.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,000.00
inventory 250mg
10-20 days ฿35,200.00
inventory 1g
10-20 days ฿72,000.00

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2-Propen-1-one, 1,3-bis(4-fluorophenyl)-3-hydroxy-
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory, antidiabetic, anticancer, and antimicrobial agents. The fluorine and hydroxyl groups in its structure enhance biological activity and support the formation of chalcone derivatives. It is also employed in research on smart materials and chemical sensors due to its responsiveness to environmental changes, such as light or pH. Commonly used in research settings to explore new therapeut

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory, antidiabetic, anticancer, and antimicrobial agents. The fluorine and hydroxyl groups in its structure enhance biological activity and support the formation of chalcone derivatives. It is also employed in research on smart materials and chemical sensors due to its responsiveness to environmental changes, such as light or pH. Commonly used in research settings to explore new therapeutic molecules and advanced materials owing to the reactivity of its carbonyl and hydroxyl groups.

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