2-Bromo-3-methyl-4-(trifluoromethyl)pyridine
95%
- Product Code: 43192
CAS:
1448776-78-0
| Molecular Weight: | 240.02 g./mol | Molecular Formula: | C₇H₅BrF₃N |
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| EC Number: | MDL Number: | MFCD26516444 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,806.00 |
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2-Bromo-3-methyl-4-(trifluoromethyl)pyridine
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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