3-Chloro-2-iodo-4-(trifluoromethoxy)aniline
95%
- Product Code: 63927
CAS:
1792885-92-7
| Molecular Weight: | 337.47 g./mol | Molecular Formula: | C₇H₄ClF₃INO |
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| Melting Point: | Boiling Point: | 299.1±40.0°C | |
| Density: | Storage Condition: | 2-8°C |
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 unique structure, featuring both chloro and iodo substituents along with a trifluoromethoxy group, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. Researchers often employ it in the synthesis of compounds that require specific halogenated aromatic frameworks, which are crucial for achieving desired biological activities. Additionally, it is used in the creation of advanced materials, where its properties can contribute to the development of novel polymers or coatings with specialized functionalities. Its role in cross-coupling reactions is also noteworthy, as it facilitates the formation of carbon-carbon bonds, a fundamental process in organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | Ft138,339.55 |
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3-Chloro-2-iodo-4-(trifluoromethoxy)aniline
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 unique structure, featuring both chloro and iodo substituents along with a trifluoromethoxy group, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. Researchers often employ it in the synthesis of compounds that require specific halogenated aromatic frameworks, which are crucial for achieving desired biological activities. Additionally, it is used in the creation of advanced materials, where its properties can contribute to the development of novel polymers or coatings with specialized functionalities. Its role in cross-coupling reactions is also noteworthy, as it facilitates the formation of carbon-carbon bonds, a fundamental process in organic chemistry.
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