4-bromo-2,5-difluorobenzonitrile
98%
- Product Code: 79064
CAS:
133541-45-4
| Molecular Weight: | 218.01 g./mol | Molecular Formula: | C₇H₂BrF₂N |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its unique structure, featuring both bromine and fluorine substituents, makes it a versatile building block for creating compounds with potential biological activity. In pharmaceuticals, it can be utilized in the development of drugs targeting specific enzymes or receptors, particularly in the design of kinase inhibitors or other small-molecule therapeutics. In agrochemicals, it serves as a precursor for the production of herbicides, fungicides, or insecticides, where the presence of halogen atoms enhances the compound's reactivity and binding affinity to biological targets. Additionally, its nitrile group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties for specific applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿414.00 |
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| 1.000 | 10-20 days | ฿909.00 |
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| 5.000 | 10-20 days | ฿3,384.00 |
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4-bromo-2,5-difluorobenzonitrile
This compound is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its unique structure, featuring both bromine and fluorine substituents, makes it a versatile building block for creating compounds with potential biological activity. In pharmaceuticals, it can be utilized in the development of drugs targeting specific enzymes or receptors, particularly in the design of kinase inhibitors or other small-molecule therapeutics. In agrochemicals, it serves as a precursor for the production of herbicides, fungicides, or insecticides, where the presence of halogen atoms enhances the compound's reactivity and binding affinity to biological targets. Additionally, its nitrile group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties for specific applications.
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