Methyl 3-bromo-4-(difluoromethoxy)benzoate
≥95%
- Product Code: 117988
CAS:
200956-56-5
| Molecular Weight: | 281.05 g./mol | Molecular Formula: | C₉H₇BrF₂O₃ |
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| EC Number: | MDL Number: | MFCD11110884 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both a bromo and a difluoromethoxy group, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce aromatic moieties into target molecules. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, further expanding its utility in synthetic chemistry. The presence of fluorine atoms enhances the biological activity and metabolic stability of the resulting compounds, making it a valuable building block in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,700.00 |
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| 0.250 | 10-20 days | ฿5,400.00 |
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Methyl 3-bromo-4-(difluoromethoxy)benzoate
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both a bromo and a difluoromethoxy group, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce aromatic moieties into target molecules. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, further expanding its utility in synthetic chemistry. The presence of fluorine atoms enhances the biological activity and metabolic stability of the resulting compounds, making it a valuable building block in drug discovery and development.
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