4-Bromo-2-(trifluoromethoxy)iodobenzene
97%
- Product Code: 79116
CAS:
175278-12-3
| Molecular Weight: | 366.90 g./mol | Molecular Formula: | C₇H₃BrF₃IO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00179334 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. Its unique structure, featuring bromine, iodine, and a trifluoromethoxy group, makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. The trifluoromethoxy group, in particular, enhances the lipophilicity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, it serves as an intermediate in the synthesis of advanced materials and specialty chemicals, where its halogenated aromatic core can be further functionalized. Its applications are particularly prominent in the development of biologically active compounds and in the field of medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white to yellow solid |
| PURITY | 96.5-100 |
| Proton NMR spectrum | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft6,679.95 |
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| 5.000 | 10-20 days | Ft12,713.45 |
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| 25.000 | 10-20 days | Ft41,157.09 |
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4-Bromo-2-(trifluoromethoxy)iodobenzene
This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. Its unique structure, featuring bromine, iodine, and a trifluoromethoxy group, makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. The trifluoromethoxy group, in particular, enhances the lipophilicity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, it serves as an intermediate in the synthesis of advanced materials and specialty chemicals, where its halogenated aromatic core can be further functionalized. Its applications are particularly prominent in the development of biologically active compounds and in the field of medicinal chemistry.
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