6-Bromo-2-(trifluoromethyl)benzo[d]oxazole
95%
- Product Code: 49852
CAS:
1260834-26-1
| Molecular Weight: | 266.0147 g./mol | Molecular Formula: | C₈H₃BrF₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring both a bromo and a trifluoromethyl group, makes it particularly valuable in pharmaceutical research. The bromo group allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the creation of diverse drug candidates. The trifluoromethyl group, known for its electron-withdrawing properties, can enhance the metabolic stability and bioavailability of pharmaceutical compounds. Additionally, this chemical is employed in the synthesis of agrochemicals, where its unique structure contributes to the development of active ingredients with improved efficacy. Its application also extends to materials science, where it is used to design advanced materials with specific electronic or optical properties. Overall, this compound plays a crucial role in the development of innovative products across various industries.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $256.76 |
+
-
|
6-Bromo-2-(trifluoromethyl)benzo[d]oxazole
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring both a bromo and a trifluoromethyl group, makes it particularly valuable in pharmaceutical research. The bromo group allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the creation of diverse drug candidates. The trifluoromethyl group, known for its electron-withdrawing properties, can enhance the metabolic stability and bioavailability of pharmaceutical compounds. Additionally, this chemical is employed in the synthesis of agrochemicals, where its unique structure contributes to the development of active ingredients with improved efficacy. Its application also extends to materials science, where it is used to design advanced materials with specific electronic or optical properties. Overall, this compound plays a crucial role in the development of innovative products across various industries.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :