2-(4-Bromophenyl)-1-(2,4-dihydroxyphenyl)ethanone

95%

Reagent Code: #151079
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CAS Number 92152-60-8

science Other reagents with same CAS 92152-60-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.14 g/mol
Formula C₁₄H₁₁BrO₃
badge Registry Numbers
MDL Number MFCD00499092
thermostat Physical Properties
Melting Point 176–177 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Shows potential in the development of antimicrobial and anti-inflammatory agents due to its structural similarity to flavonoids. Also employed in research settings for studying kinase inhibition and antioxidant activity. Its brominated aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,720.00
inventory 1g
10-20 days ฿5,420.00
inventory 5g
10-20 days ฿18,940.00

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2-(4-Bromophenyl)-1-(2,4-dihydroxyphenyl)ethanone
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Shows potential in the development of antimicrobial and anti-inflammatory agents due to its structural similarity to flavonoids. Also employed in research settings for studying kinase inhibition and antioxidant activity. Its brominated aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery.

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Shows potential in the development of antimicrobial and anti-inflammatory agents due to its structural similarity to flavonoids. Also employed in research settings for studying kinase inhibition and antioxidant activity. Its brominated aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery.

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