5-Bromo-2-(2,2,2-trifluoroethyl)pyridine

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Reagent Code: #48880
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CAS Number 1335050-19-5

science Other reagents with same CAS 1335050-19-5

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Weight 240.0200 g/mol
Formula C₇H₅NF₃Br
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Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring both a bromine atom and a trifluoroethyl group, makes it particularly valuable in the creation of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the introduction of various substituents. Additionally, the trifluoroethyl group can enhance the biological activity and metabolic stability of the resulting compounds, making it a key component in the design of drug candidates. It is also explored in the synthesis of advanced materials, where its unique properties can contribute to the development of novel polymers or coatings with specialized characteristics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,750.00

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

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring both a bromine atom and a trifluoroethyl group, makes it particularly valuable in the creation of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the introduction of various substituents. Additionally, the trifluoroethyl group can enhance the biological activity and metabolic stability of the resulting compounds, making it a key component in the design of drug candidates. It is also explored in the synthesis of advanced materials, where its unique properties can contribute to the development of novel polymers or coatings with specialized characteristics.

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