4-Bromo-2-(trifluoromethyl)benzo[d]thiazole
97%
- Product Code: 87001
CAS:
1188136-39-1
| Molecular Weight: | 282.08 g./mol | Molecular Formula: | C₈H₃BrF₃NS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11217356 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique combination of bromine and trifluoromethyl groups on the benzo[d]thiazole ring makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and advanced materials. In medicinal chemistry, it serves as a key intermediate for designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Additionally, its electron-withdrawing properties are exploited in the synthesis of dyes, fluorescent markers, and other functional materials. The compound's stability and reactivity also make it suitable for use in cross-coupling reactions, enabling the construction of diverse aromatic systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,145.00 |
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| 0.250 | 10-20 days | ฿13,842.00 |
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| 1.000 | 10-20 days | ฿37,359.00 |
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4-Bromo-2-(trifluoromethyl)benzo[d]thiazole
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique combination of bromine and trifluoromethyl groups on the benzo[d]thiazole ring makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and advanced materials. In medicinal chemistry, it serves as a key intermediate for designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Additionally, its electron-withdrawing properties are exploited in the synthesis of dyes, fluorescent markers, and other functional materials. The compound's stability and reactivity also make it suitable for use in cross-coupling reactions, enabling the construction of diverse aromatic systems.
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