4-(4-Bromophenyl)but-3-en-2-one

95%

Reagent Code: #149203
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CAS Number 3815-31-4

science Other reagents with same CAS 3815-31-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.08 g/mol
Formula C₁₀H₉BrO
badge Registry Numbers
MDL Number MFCD00174096
thermostat Physical Properties
Boiling Point 321.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of chalcone derivatives which exhibit biological activities such as antimicrobial, anti-inflammatory, and anticancer properties. It serves as a building block in the development of pharmaceuticals and agrochemicals due to its reactive α,β-unsaturated ketone functionality. The compound is also employed in cross-coupling reactions, enabling the construction of complex aromatic systems for materials science and medicinal chemistry applications. Its conjugated structure makes it useful in studies involving Michael additions and cyclization reactions to form heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,670.00
inventory 1g
10-20 days ฿3,260.00
inventory 5g
10-20 days ฿16,210.00
inventory 10g
10-20 days ฿28,150.00

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4-(4-Bromophenyl)but-3-en-2-one
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Used as a key intermediate in organic synthesis, particularly in the preparation of chalcone derivatives which exhibit biological activities such as antimicrobial, anti-inflammatory, and anticancer properties. It serves as a building block in the development of pharmaceuticals and agrochemicals due to its reactive α,β-unsaturated ketone functionality. The compound is also employed in cross-coupling reactions, enabling the construction of complex aromatic systems for materials science and medicinal chemis

Used as a key intermediate in organic synthesis, particularly in the preparation of chalcone derivatives which exhibit biological activities such as antimicrobial, anti-inflammatory, and anticancer properties. It serves as a building block in the development of pharmaceuticals and agrochemicals due to its reactive α,β-unsaturated ketone functionality. The compound is also employed in cross-coupling reactions, enabling the construction of complex aromatic systems for materials science and medicinal chemistry applications. Its conjugated structure makes it useful in studies involving Michael additions and cyclization reactions to form heterocyclic compounds.

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