1-Iodo-3-(trifluoromethoxy)benzene
98%
- Product Code: 114886
Alias:
α,α,α-Trifluoro-3-iodoanisole
CAS:
198206-33-6
| Molecular Weight: | 288.01 g./mol | Molecular Formula: | C₆H₄OCF₃I |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01090992 | |
| Melting Point: | Boiling Point: | 185-186 °C(lit.) | |
| Density: | 1.863 g/mL at 25 °C(lit.) | Storage Condition: | room temperature, away from light |
Product Description:
1-Iodo-3-(trifluoromethoxy)benzene is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both an iodine atom and a trifluoromethoxy group, makes it valuable for introducing these functional groups into more complex molecules. The iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the construction of diverse aromatic compounds. The trifluoromethoxy group is often incorporated into drug molecules to enhance their metabolic stability, lipophilicity, and binding affinity to biological targets. Additionally, this compound is employed in material science for the synthesis of advanced materials, including liquid crystals and polymers, where the unique electronic properties of the trifluoromethoxy group can be leveraged. Its applications are crucial in fields requiring precise molecular modifications to achieve desired chemical and physical properties.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 98-100 |
| Refractive Index N20/D | 1.503-1.507 |
| Specific Gravity (20/20) | 1.867-1.871 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿320.00 |
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| 5.000 | 10-20 days | ฿990.00 |
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| 25.000 | 10-20 days | ฿1,950.00 |
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| 100.000 | 10-20 days | ฿6,260.00 |
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1-Iodo-3-(trifluoromethoxy)benzene
1-Iodo-3-(trifluoromethoxy)benzene is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both an iodine atom and a trifluoromethoxy group, makes it valuable for introducing these functional groups into more complex molecules. The iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the construction of diverse aromatic compounds. The trifluoromethoxy group is often incorporated into drug molecules to enhance their metabolic stability, lipophilicity, and binding affinity to biological targets. Additionally, this compound is employed in material science for the synthesis of advanced materials, including liquid crystals and polymers, where the unique electronic properties of the trifluoromethoxy group can be leveraged. Its applications are crucial in fields requiring precise molecular modifications to achieve desired chemical and physical properties.
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