Ethyl 4-bromo-3,5-diethoxybenzoate
≥95%
- Product Code: 119316
CAS:
149517-92-0
| Molecular Weight: | 317.18 g./mol | Molecular Formula: | C₁₃H₁₇BrO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11977359 | |
| Melting Point: | Boiling Point: | 390.038°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a bromine atom and ethoxy groups, makes it a valuable building block in the development of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse aromatic compounds. Additionally, the ethoxy groups can be modified or removed, providing flexibility in designing target molecules. It is also employed in research settings for studying reaction mechanisms and developing new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,233.00 |
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| 0.250 | 10-20 days | ฿1,935.00 |
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| 1.000 | 10-20 days | ฿4,977.00 |
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Ethyl 4-bromo-3,5-diethoxybenzoate
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a bromine atom and ethoxy groups, makes it a valuable building block in the development of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse aromatic compounds. Additionally, the ethoxy groups can be modified or removed, providing flexibility in designing target molecules. It is also employed in research settings for studying reaction mechanisms and developing new synthetic methodologies.
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