2-(2-bromopyridin-4-yl)-1-(4-fluorophenyl)ethanone
95%
Reagent
Code: #82320
CAS Number
158876-70-1
blur_circular Chemical Specifications
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Molecular Information
Weight
294.12 g/mol
Formula
C₁₃H₉BrFNO
thermostat
Physical Properties
Melting Point
112 °C
Boiling Point
420.1±35.0 °C(Predicted)
inventory_2
Storage & Handling
Density
1.506±0.06 g/cm3(Predicted)
Storage
room temperature
description Product Description
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of various pharmaceutical agents. Its structure, featuring both a bromopyridine and a fluorophenyl group, makes it particularly valuable for constructing complex molecules with potential biological activity. Researchers often employ it in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create novel compounds for drug discovery. Additionally, its presence in medicinal chemistry is notable for the design of molecules targeting specific enzymes or receptors, particularly in the development of central nervous system (CNS) drugs or anti-inflammatory agents. Its unique combination of functional groups also allows for further derivatization, enabling the exploration of diverse chemical spaces in search of new therapeutic candidates.
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2-(2-bromopyridin-4-yl)-1-(4-fluorophenyl)ethanone
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of various pharmaceutical agents. Its structure, featuring both a bromopyridine and a fluorophenyl group, makes it particularly valuable for constructing complex molecules with potential biological activity. Researchers often employ it in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create novel compounds for drug discovery. Additionally, its presence in medicinal chemistry is notable for the design of molecules targeting specific enzymes or receptors, particularly in the development of central nervous system (CNS) drugs or anti-inflammatory agents. Its unique combination of functional groups also allows for further derivatization, enabling the exploration of diverse chemical spaces in search of new therapeutic candidates.
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