3-Bromo-5-chloro-2-(trifluoromethyl)pyridine
97%
- Product Code: 45272
CAS:
823222-22-6
| Molecular Weight: | 260.4500 g./mol | Molecular Formula: | C₆H₂BrClF₃N |
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| EC Number: | MDL Number: | MFCD11847355 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its unique structure, featuring bromo, chloro, and trifluoromethyl groups, makes it a versatile building block for the development of active pharmaceutical ingredients (APIs) and crop protection agents. In pharmaceuticals, it is often employed in the creation of compounds targeting specific biological pathways, particularly in the development of drugs with anti-inflammatory, antiviral, or anticancer properties. In agrochemicals, it serves as a precursor for the production of herbicides, fungicides, and insecticides, where the trifluoromethyl group enhances the efficacy and stability of the final product. Additionally, its reactivity allows for further functionalization, making it valuable in organic synthesis and research applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £148.39 |
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3-Bromo-5-chloro-2-(trifluoromethyl)pyridine
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its unique structure, featuring bromo, chloro, and trifluoromethyl groups, makes it a versatile building block for the development of active pharmaceutical ingredients (APIs) and crop protection agents. In pharmaceuticals, it is often employed in the creation of compounds targeting specific biological pathways, particularly in the development of drugs with anti-inflammatory, antiviral, or anticancer properties. In agrochemicals, it serves as a precursor for the production of herbicides, fungicides, and insecticides, where the trifluoromethyl group enhances the efficacy and stability of the final product. Additionally, its reactivity allows for further functionalization, making it valuable in organic synthesis and research applications.
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