5-Iodo-3-(trifluoromethyl)pyridin-2-amine
97%
- Product Code: 49296
CAS:
911112-05-5
| Molecular Weight: | 288.0100 g./mol | Molecular Formula: | C₆H₄F₃IN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16250855 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an iodine atom and a trifluoromethyl group, makes it particularly valuable for creating molecules with potential biological activity.
In medicinal chemistry, it is often employed in the construction of complex molecules targeting specific diseases, such as cancer, neurological disorders, and infectious diseases. The presence of the trifluoromethyl group can enhance the metabolic stability and bioavailability of the resulting compounds, while the iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira reactions.
Additionally, this chemical is used in agrochemical research to develop novel pesticides and herbicides, leveraging its unique structural properties to improve efficacy and selectivity. Its versatility and reactivity make it a valuable tool in the design and optimization of new chemical entities across various industries.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,295.00 |
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5-Iodo-3-(trifluoromethyl)pyridin-2-amine
This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an iodine atom and a trifluoromethyl group, makes it particularly valuable for creating molecules with potential biological activity.
In medicinal chemistry, it is often employed in the construction of complex molecules targeting specific diseases, such as cancer, neurological disorders, and infectious diseases. The presence of the trifluoromethyl group can enhance the metabolic stability and bioavailability of the resulting compounds, while the iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira reactions.
Additionally, this chemical is used in agrochemical research to develop novel pesticides and herbicides, leveraging its unique structural properties to improve efficacy and selectivity. Its versatility and reactivity make it a valuable tool in the design and optimization of new chemical entities across various industries.
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