2-(trifluoromethyl)thiazol-5-amine
95%
- Product Code: 41850
CAS:
1367944-72-6
| Molecular Weight: | 168.1402296 g./mol | Molecular Formula: | C₄H₃F₃N₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 164.6±40.0 ℃ at 760 mmHg | |
| Density: | 1.557±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the pharmaceutical and agrochemical industries due to its unique structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting infectious diseases and metabolic disorders. Its trifluoromethyl group enhances the bioavailability and stability of the resulting compounds, making it valuable in drug development.
In agrochemicals, it is employed in the creation of pesticides and herbicides. The thiazole ring and trifluoromethyl group contribute to the efficacy of these products by improving their ability to target specific pests or weeds while minimizing environmental impact. Additionally, its chemical structure allows for the development of compounds with enhanced resistance to degradation, ensuring longer-lasting effects in agricultural applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,032.00 |
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| 0.100 | 10-20 days | ฿4,131.00 |
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| 0.250 | 10-20 days | ฿9,873.00 |
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| 1.000 | 10-20 days | ฿27,360.00 |
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2-(trifluoromethyl)thiazol-5-amine
This chemical is primarily utilized in the pharmaceutical and agrochemical industries due to its unique structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting infectious diseases and metabolic disorders. Its trifluoromethyl group enhances the bioavailability and stability of the resulting compounds, making it valuable in drug development.
In agrochemicals, it is employed in the creation of pesticides and herbicides. The thiazole ring and trifluoromethyl group contribute to the efficacy of these products by improving their ability to target specific pests or weeds while minimizing environmental impact. Additionally, its chemical structure allows for the development of compounds with enhanced resistance to degradation, ensuring longer-lasting effects in agricultural applications.
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