Methyl 2-bromo-3,6-difluorobenzoate
97%
- Product Code: 116634
CAS:
1805523-44-7
| Molecular Weight: | 251.02 g./mol | Molecular Formula: | C₈H₅BrF₂O₂ |
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| EC Number: | MDL Number: | MFCD28061358 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure, featuring both bromine and fluorine substituents, makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse aromatic compounds. Additionally, the fluorine atoms can enhance the stability and bioavailability of the resulting molecules, which is particularly useful in drug discovery. This compound is also employed in research settings to study the effects of halogenated aromatic systems in chemical reactions and material properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,314.00 |
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| 0.250 | 10-20 days | ฿2,115.00 |
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| 1.000 | 10-20 days | ฿5,265.00 |
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| 5.000 | 10-20 days | ฿16,137.00 |
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Methyl 2-bromo-3,6-difluorobenzoate
This chemical is primarily used in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure, featuring both bromine and fluorine substituents, makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse aromatic compounds. Additionally, the fluorine atoms can enhance the stability and bioavailability of the resulting molecules, which is particularly useful in drug discovery. This compound is also employed in research settings to study the effects of halogenated aromatic systems in chemical reactions and material properties.
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