1-[4-(3-Bromoprop-1-yn-1-yl)phenyl]ethan-1-one

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Reagent Code: #131479
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CAS Number 731785-24-3

science Other reagents with same CAS 731785-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.09 g/mol
Formula C₁₁H₉BrO
badge Registry Numbers
MDL Number MFCD30477342
thermostat Physical Properties
Boiling Point 321.9±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.43±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its alkyne functionality allows for use in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in drug discovery and development. The bromo group provides a site for further functionalization via cross-coupling reactions like Suzuki or Sonogashira couplings. It is also employed in the synthesis of kinase inhibitors and other targeted therapeutic agents. Its structural features make it valuable in building complex aromatic and conjugated systems for materials science and medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,110.00
inventory 250mg
10-20 days ฿26,210.00

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1-[4-(3-Bromoprop-1-yn-1-yl)phenyl]ethan-1-one
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its alkyne functionality allows for use in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in drug discovery and development. The bromo group provides a site for further functionalization via cross-coupling reactions like Suzuki or Sonogashira couplings. It is also employed in the synthesis of kinase inhibitors and

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its alkyne functionality allows for use in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in drug discovery and development. The bromo group provides a site for further functionalization via cross-coupling reactions like Suzuki or Sonogashira couplings. It is also employed in the synthesis of kinase inhibitors and other targeted therapeutic agents. Its structural features make it valuable in building complex aromatic and conjugated systems for materials science and medicinal chemistry applications.

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