1-Bromo-4-iodo-2-(trifluoromethoxy)benzene
97%
- Product Code: 114790
CAS:
1187984-18-4
| Molecular Weight: | 366.90 g./mol | Molecular Formula: | C₇H₃BrF₃IO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12761590 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both bromine and iodine substituents, makes it highly reactive in cross-coupling reactions, such as Suzuki, Sonogashira, and Heck couplings, which are essential in pharmaceutical and material science research. The trifluoromethoxy group enhances the electron-withdrawing properties, making it valuable in the design of compounds with specific electronic characteristics. It is often employed in the synthesis of agrochemicals, pharmaceuticals, and advanced materials, where precise molecular modifications are required. Additionally, its halogenated aromatic structure is useful in the study of reaction mechanisms and in the preparation of intermediates for further functionalization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,233.00 |
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| 0.250 | 10-20 days | ฿2,448.00 |
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1-Bromo-4-iodo-2-(trifluoromethoxy)benzene
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both bromine and iodine substituents, makes it highly reactive in cross-coupling reactions, such as Suzuki, Sonogashira, and Heck couplings, which are essential in pharmaceutical and material science research. The trifluoromethoxy group enhances the electron-withdrawing properties, making it valuable in the design of compounds with specific electronic characteristics. It is often employed in the synthesis of agrochemicals, pharmaceuticals, and advanced materials, where precise molecular modifications are required. Additionally, its halogenated aromatic structure is useful in the study of reaction mechanisms and in the preparation of intermediates for further functionalization.
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