1-(4-bromophenyl)-2-phenylethane-1,2-dione
98%
Reagent
Code: #148029
CAS Number
39229-12-4
blur_circular Chemical Specifications
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Molecular Information
Weight
289.1241 g/mol
Formula
C₁₄H₉BrO₂
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Registry Numbers
MDL Number
MFCD00223484
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Physical Properties
Melting Point
86.5℃
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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.
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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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