In the synthetic process, it provides the required para-substituted aromatic ring that becomes part of the atazanavir molecular framework. The aldehyde functional group participates in carbon–carbon bond-forming reactions to construct important side-chain intermediates, while the bromo substituent enables further chemical transformations such as coupling reactions. Because of its suitable reactivity and well-defined substitution pattern, 4-bromobenzaldehyde plays a direct and important role in the efficient synthesis of atazanavir. 4-Bromobenzaldehyde serves as a key starting material and intermediate in the synthesis of atazanavir, an antiretroviral protease inhibitor.
4-Bromobenzaldehyde
| API Name | Atazanavir |
|---|---|
| CAS No | 1122-91-4 |
| Molecular Formula | C7H5BrO |
| Molecular Weight | 185.02 g/mol |
| Synonyms | 4-bromobenzaldehyde |
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