4-Benzyl-2-phenyloxazol-5(4H)-one

97%

Reagent Code: #148283
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CAS Number 5874-61-3

science Other reagents with same CAS 5874-61-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.28 g/mol
Formula C₁₆H₁₃NO₂
badge Registry Numbers
MDL Number MFCD00157349
thermostat Physical Properties
Boiling Point 375.4°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.17g/cm3
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It serves as a building block in the development of heterocyclic compounds due to its oxazolone core, which is known for reactivity in ring-opening and cycloaddition reactions. Employed in the synthesis of certain anticonvulsant and anti-inflammatory agents. Also utilized in research settings for the development of novel organic molecules with potential therapeutic applications.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,230.00
inventory 1g
10-20 days ฿6,350.00

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4-Benzyl-2-phenyloxazol-5(4H)-one
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It serves as a building block in the development of heterocyclic compounds due to its oxazolone core, which is known for reactivity in ring-opening and cycloaddition reactions. Employed in the synthesis of certain anticonvulsant and anti-inflammatory agents. Also utilized in research settings for the development of novel organic molecules with potential therapeutic applicati

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It serves as a building block in the development of heterocyclic compounds due to its oxazolone core, which is known for reactivity in ring-opening and cycloaddition reactions. Employed in the synthesis of certain anticonvulsant and anti-inflammatory agents. Also utilized in research settings for the development of novel organic molecules with potential therapeutic applications.

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