1-Chloro-2-iodo-3-(trifluoromethyl)benzene
97%
- Product Code: 79444
CAS:
203626-41-9
| Molecular Weight: | 306.45 g./mol | Molecular Formula: | C₇H₃ClF₃I |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00673987 | |
| Melting Point: | Boiling Point: | 225.5°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, 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 complex molecules. Its unique structure, featuring both chloro and iodo substituents along with a trifluoromethyl group, makes it particularly valuable in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. Additionally, the trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting compounds, making it a key intermediate in the design of biologically active molecules, including potential drug candidates. It is also employed in material science for the synthesis of advanced polymers and liquid crystals, where the presence of halogen atoms and the trifluoromethyl group can impart specific electronic and optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿873.00 |
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| 1.000 | 10-20 days | ฿3,249.00 |
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| 5.000 | 10-20 days | ฿16,200.00 |
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1-Chloro-2-iodo-3-(trifluoromethyl)benzene
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of complex molecules. Its unique structure, featuring both chloro and iodo substituents along with a trifluoromethyl group, makes it particularly valuable in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. Additionally, the trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting compounds, making it a key intermediate in the design of biologically active molecules, including potential drug candidates. It is also employed in material science for the synthesis of advanced polymers and liquid crystals, where the presence of halogen atoms and the trifluoromethyl group can impart specific electronic and optical properties.
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