2-Bromo-4-(trifluoromethoxy)benzaldehyde
98%
- Product Code: 124077
CAS:
1114808-87-5
| Molecular Weight: | 269.02 g./mol | Molecular Formula: | C₈H₄BrF₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09835093 | |
| Melting Point: | Boiling Point: | 509.0±50.0 °C(Predicted) | |
| Density: | 1.19±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both a bromine atom and a trifluoromethoxy group, makes it valuable for constructing complex molecules with specific biological activities. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic aldehyde functionalities into target compounds. Additionally, it serves as a key building block in the development of active ingredients for herbicides, fungicides, and other crop protection agents. Its trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting molecules, making it particularly useful in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $216.98 |
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| 1.000 | 10-20 days | $332.24 |
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| 5.000 | 10-20 days | $1,018.88 |
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2-Bromo-4-(trifluoromethoxy)benzaldehyde
This compound is primarily utilized in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both a bromine atom and a trifluoromethoxy group, makes it valuable for constructing complex molecules with specific biological activities. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic aldehyde functionalities into target compounds. Additionally, it serves as a key building block in the development of active ingredients for herbicides, fungicides, and other crop protection agents. Its trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting molecules, making it particularly useful in drug discovery and development.
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