1-bromo-3,4-difluoro-2-methoxybenzene
95%
- Product Code: 114751
CAS:
888318-22-7
| Molecular Weight: | 223.0148 g./mol | Molecular Formula: | C₇H₅BrF₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16295239 | |
| Melting Point: | Boiling Point: | 195.7±35.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs) or drug candidates. The presence of bromine, fluorine, and methoxy groups allows for selective functionalization, making it useful in cross-coupling reactions like Suzuki or Buchwald-Hartwig reactions. Additionally, it finds application in material science, where it is employed in the creation of specialty chemicals or advanced polymers with specific electronic or structural properties. Its unique substitution pattern also makes it a candidate for agrochemical research, aiding in the development of novel pesticides or herbicides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,197.00 |
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| 1.000 | 10-20 days | ฿2,349.00 |
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1-bromo-3,4-difluoro-2-methoxybenzene
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs) or drug candidates. The presence of bromine, fluorine, and methoxy groups allows for selective functionalization, making it useful in cross-coupling reactions like Suzuki or Buchwald-Hartwig reactions. Additionally, it finds application in material science, where it is employed in the creation of specialty chemicals or advanced polymers with specific electronic or structural properties. Its unique substitution pattern also makes it a candidate for agrochemical research, aiding in the development of novel pesticides or herbicides.
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