In the synthetic route, it acts as an alkylating agent, introducing the 2-methylpropionyl fragment onto the nitrogen of the intermediate thiohydantoin or related amine structure. This step is crucial for forming the correct N-substituted scaffold that contributes to the biological activity of Enzalutamide. After this alkylation, further transformations such as cyclization, coupling, or purification steps lead to the formation of the final Active Pharmaceutical Ingredient. 2-Bromo-2-methylpropanoic acid is an important intermediate in the synthesis of Enzalutamide.
2-Bromo-2-methylpropanoic acid
| API Name | Enzalutamide |
|---|---|
| CAS No | 2052-01-9 |
| Molecular Formula | C4H7BrO2 |
| Molecular Weight | 167.00 g/mol |
| Synonyms | 2-bromo-2-methylpropanoic acid |
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Frequently Asked Questions
In the synthetic route, it acts as an alkylating agent, introducing the 2-methylpropionyl fragment onto the nitrogen of the intermediate thiohydantoin or related amine structure. This step is crucial for forming the correct N-substituted scaffold that contributes to the biological activity of Enzalutamide. After this alkylation, further transformations such as cyclization, coupling, or purification steps lead to the formation of the final Active Pharmaceutical Ingredient. 2-Bromo-2-methylpropanoic acid is an important intermediate in the synthesis of Enzalutamide.
The CAS number of 2-Bromo-2-methylpropanoic acid is 2052-01-9.
The molecular formula of 2-Bromo-2-methylpropanoic acid is C4H7BrO2.
The listed molecular weight of 2-Bromo-2-methylpropanoic acid is 167.00 g/mol.
2-Bromo-2-methylpropanoic acid is listed as being used in connection with the following API: Enzalutamide.
The listed synonym or IUPAC name for 2-Bromo-2-methylpropanoic acid is 2-bromo-2-methylpropanoic acid.