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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Frequently Asked Questions
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.
The CAS number of 4-Bromobenzaldehyde is 1122-91-4.
The molecular formula of 4-Bromobenzaldehyde is C7H5BrO.
The listed molecular weight of 4-Bromobenzaldehyde is 185.02 g/mol.
4-Bromobenzaldehyde is listed as being used in connection with the following API: Atazanavir.
The listed synonym or IUPAC name for 4-Bromobenzaldehyde is 4-bromobenzaldehyde.