Methyl 4-bromo-3-carbamoylbenzoate
98%
- Product Code: 203979
CAS:
2140305-53-7
| Molecular Weight: | 258.07 g./mol | Molecular Formula: | C₉H₈BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30834356 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—ester, bromo, and carbamoyl—allow for selective modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine atom serves as a reactive site for carbon-carbon bond formation. Also utilized in the preparation of heterocyclic compounds through cyclization strategies, supporting research in medicinal chemistry for lead optimization and drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | €131.25 |
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| 250mg | 10-20 days | €230.93 |
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| 1g | 10-20 days | €653.60 |
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Methyl 4-bromo-3-carbamoylbenzoate
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—ester, bromo, and carbamoyl—allow for selective modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine atom serves as a reactive site for carbon-carbon bond formation. Also utilized in the preparation of heterocyclic compounds through cyclization strategies, supporting research in medicinal chemistry for lead optimization and drug discovery.
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