1-Bromo-3-(difluoromethoxy)-5-nitrobenzene
95%
- Product Code: 40014
CAS:
1261441-47-7
| Molecular Weight: | 268.0100 g./mol | Molecular Formula: | C₇H₄BrF₂NO₃ |
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| EC Number: | MDL Number: | MFCD18390953 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of more complex molecules. Its unique structure, featuring bromine, difluoromethoxy, and nitro groups, 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 couplings, to introduce aromatic functionalities into target molecules. Additionally, its nitro group can be reduced to an amine, opening pathways for further functionalization. Researchers also explore its potential in material science, particularly in the synthesis of advanced polymers and coatings with specific electronic or optical properties. Its fluorine-containing moiety can enhance the stability and bioavailability of drug candidates, making it a key component in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿5,553.00 |
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1-Bromo-3-(difluoromethoxy)-5-nitrobenzene
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of more complex molecules. Its unique structure, featuring bromine, difluoromethoxy, and nitro groups, 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 couplings, to introduce aromatic functionalities into target molecules. Additionally, its nitro group can be reduced to an amine, opening pathways for further functionalization. Researchers also explore its potential in material science, particularly in the synthesis of advanced polymers and coatings with specific electronic or optical properties. Its fluorine-containing moiety can enhance the stability and bioavailability of drug candidates, making it a key component in medicinal chemistry.
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