1-(4-bromophenyl)-2-phenylethane-1,2-dione

98%

Reagent Code: #148029
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CAS Number 39229-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.1241 g/mol
Formula C₁₄H₉BrO₂
badge Registry Numbers
MDL Number MFCD00223484
thermostat Physical Properties
Melting Point 86.5℃
inventory_2 Storage & Handling
Density 1.47 g/ml
Storage Room temperature, dry, sealed

description Product Description

Used primarily as a synthetic intermediate in organic chemistry, this compound plays a key role in the construction of complex aromatic and heterocyclic systems. Its dual carbonyl functionality allows for selective reactions, making it valuable in the synthesis of pharmaceuticals and bioactive molecules. It is often employed in condensation reactions to form flavonoids, chalcones, and other conjugated systems with potential antimicrobial or anti-inflammatory activity. Additionally, it serves as a building block in the preparation of photolabile protecting groups and fluorescent probes due to its distinct electronic properties. Its bromo substituent enables further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, expanding its utility in medicinal chemistry and materials science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,290.00
inventory 1g
10-20 days ฿9,850.00
inventory 5g
10-20 days ฿34,430.00
1-(4-bromophenyl)-2-phenylethane-1,2-dione
Used primarily as a synthetic intermediate in organic chemistry, this compound plays a key role in the construction of complex aromatic and heterocyclic systems. Its dual carbonyl functionality allows for selective reactions, making it valuable in the synthesis of pharmaceuticals and bioactive molecules. It is often employed in condensation reactions to form flavonoids, chalcones, and other conjugated systems with potential antimicrobial or anti-inflammatory activity. Additionally, it serves as a building block in the preparation of photolabile protecting groups and fluorescent probes due to its distinct electronic properties. Its bromo substituent enables further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, expanding its utility in medicinal chemistry and materials science.
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