1-Bromo-2,3-bis(trifluoromethyl)benzene

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Reagent Code: #39982
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CAS Number 1192548-06-3

science Other reagents with same CAS 1192548-06-3

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Weight 293.0038 g/mol
Formula C₈H₃BrF₆
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This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring bromine and trifluoromethyl groups, makes it a valuable intermediate for creating molecules with specific electronic and steric properties. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic rings with trifluoromethyl substituents into target molecules. These reactions are crucial for developing compounds with enhanced biological activity or unique physical properties. Additionally, it finds use in material science for designing advanced polymers and liquid crystals, where the trifluoromethyl groups contribute to thermal stability and chemical resistance. Its role in organic synthesis underscores its importance in producing high-performance materials and bioactive compounds.

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inventory 100mg
10-20 days ฿21,110.00

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1-Bromo-2,3-bis(trifluoromethyl)benzene
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This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring bromine and trifluoromethyl groups, makes it a valuable intermediate for creating molecules with specific electronic and steric properties. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic rings with trifluoromethyl substituents into target molecules. These reactions are crucial for
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring bromine and trifluoromethyl groups, makes it a valuable intermediate for creating molecules with specific electronic and steric properties. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic rings with trifluoromethyl substituents into target molecules. These reactions are crucial for developing compounds with enhanced biological activity or unique physical properties. Additionally, it finds use in material science for designing advanced polymers and liquid crystals, where the trifluoromethyl groups contribute to thermal stability and chemical resistance. Its role in organic synthesis underscores its importance in producing high-performance materials and bioactive compounds.
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