(2E)-1-(4-bromophenyl)-3-(2,3,4-trimethoxyphenyl)prop-2-en-1-one

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Reagent Code: #180876
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CAS Number 2250288-68-5

science Other reagents with same CAS 2250288-68-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 377.23 g/mol
Formula C₁₈H₁₇BrO₄
thermostat Physical Properties
Boiling Point 493.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.356±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports conjugation and electron delocalization, making it valuable in the development of chalcone-based derivatives with potential anticancer, antimicrobial, and anti-inflammatory properties. Commonly employed in medicinal chemistry research to design compounds targeting enzyme inhibition and oxidative stress pathways. Also utilized in material science for studying charge transfer complexes due to the presence of electron-donating methoxy groups and a halogen substituent.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,800.00
inventory 250mg
10-20 days ฿25,600.00
inventory 1g
10-20 days ฿48,000.00

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(2E)-1-(4-bromophenyl)-3-(2,3,4-trimethoxyphenyl)prop-2-en-1-one
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports conjugation and electron delocalization, making it valuable in the development of chalcone-based derivatives with potential anticancer, antimicrobial, and anti-inflammatory properties. Commonly employed in medicinal chemistry research to design compounds targeting enzyme inhibition and oxidative stress pathways. Also utilized in material science for studying charge transfer complexes due to th

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports conjugation and electron delocalization, making it valuable in the development of chalcone-based derivatives with potential anticancer, antimicrobial, and anti-inflammatory properties. Commonly employed in medicinal chemistry research to design compounds targeting enzyme inhibition and oxidative stress pathways. Also utilized in material science for studying charge transfer complexes due to the presence of electron-donating methoxy groups and a halogen substituent.

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