4-Chloro-7-(trifluoromethoxy)quinazoline
≥95%
- Product Code: 86140
CAS:
1160994-87-5
| Molecular Weight: | 248.59 g./mol | Molecular Formula: | C₉H₄ClF₃N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12400772 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
4-Chloro-7-(trifluoromethoxy)quinazoline is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinazoline core structure is particularly valuable in the development of kinase inhibitors, which are crucial in targeting specific enzymes involved in signal transduction pathways. This compound is often employed in the design and production of potential therapeutic agents for treating diseases such as cancer, where kinase activity is dysregulated. Additionally, its unique substitution pattern, including the chloro and trifluoromethoxy groups, enhances its reactivity and selectivity in chemical reactions, making it a versatile building block for further modifications. Researchers also explore its applications in creating novel pharmaceuticals with improved efficacy and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,312.00 |
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| 0.250 | 10-20 days | ฿5,841.00 |
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| 1.000 | 10-20 days | ฿20,475.00 |
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4-Chloro-7-(trifluoromethoxy)quinazoline
4-Chloro-7-(trifluoromethoxy)quinazoline is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinazoline core structure is particularly valuable in the development of kinase inhibitors, which are crucial in targeting specific enzymes involved in signal transduction pathways. This compound is often employed in the design and production of potential therapeutic agents for treating diseases such as cancer, where kinase activity is dysregulated. Additionally, its unique substitution pattern, including the chloro and trifluoromethoxy groups, enhances its reactivity and selectivity in chemical reactions, making it a versatile building block for further modifications. Researchers also explore its applications in creating novel pharmaceuticals with improved efficacy and reduced side effects.
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