3,5-Difluoro-4-methoxybenzyl bromide
95%
- Product Code: 44026
CAS:
706786-42-7
| Molecular Weight: | 237.0414 g./mol | Molecular Formula: | C₈H₇BrF₂O |
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| EC Number: | MDL Number: | MFCD04115916 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
3,5-Difluoro-4-methoxybenzyl bromide is primarily used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and methoxy groups, makes it valuable for constructing complex molecules with specific biological activities. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the introduction of fluorine atoms can enhance metabolic stability and binding affinity. Additionally, it serves as a building block in the preparation of herbicides and pesticides, leveraging its ability to modify the electronic properties of target compounds. Its reactivity as a benzyl bromide also makes it useful in cross-coupling reactions and other transformations in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,790.00 |
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3,5-Difluoro-4-methoxybenzyl bromide
3,5-Difluoro-4-methoxybenzyl bromide is primarily used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and methoxy groups, makes it valuable for constructing complex molecules with specific biological activities. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the introduction of fluorine atoms can enhance metabolic stability and binding affinity. Additionally, it serves as a building block in the preparation of herbicides and pesticides, leveraging its ability to modify the electronic properties of target compounds. Its reactivity as a benzyl bromide also makes it useful in cross-coupling reactions and other transformations in medicinal chemistry research.
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