2-Bromo-3-methyl-4-(trifluoromethyl)pyridine

95%

Reagent Code: #43192
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CAS Number 1448776-78-0

science Other reagents with same CAS 1448776-78-0

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Weight 240.02 g/mol
Formula C₇H₅BrF₃N
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MDL Number MFCD26516444
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This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a trifluoromethyl group, makes it particularly valuable in the creation of agrochemicals and pharmaceuticals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the introduction of various substituents. The trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it a key component in the design of active ingredients for crop protection products and drug candidates. Additionally, it is employed in the synthesis of materials with specific electronic properties, contributing to advancements in organic electronics and optoelectronics.

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inventory 100mg
10-20 days ฿4,806.00

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2-Bromo-3-methyl-4-(trifluoromethyl)pyridine
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This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a trifluoromethyl group, makes it particularly valuable in the creation of agrochemicals and pharmaceuticals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the introduction of various substituents. The trifluoromethyl gro

This compound is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a trifluoromethyl group, makes it particularly valuable in the creation of agrochemicals and pharmaceuticals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the introduction of various substituents. The trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it a key component in the design of active ingredients for crop protection products and drug candidates. Additionally, it is employed in the synthesis of materials with specific electronic properties, contributing to advancements in organic electronics and optoelectronics.

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