In a common synthetic route, 3′-aminoacetophenone is converted to 3′-hydroxyacetophenone through a diazotization and hydrolysis process. The 3′-hydroxyacetophenone intermediate is then used as the primary starting material for the subsequent steps that build the final phenylephrine structure. 3′-Aminoacetophenone serves as a key pharmaceutical intermediate in one of the steps to synthesize phenylephrine hydrochloride.
3′-Aminoacetophenone
| API Name | Phenylephrine hydrochloride |
|---|---|
| CAS No | 99-03-6 |
| Molecular Formula | C8H9NO |
| Molecular Weight | 135.16 g/mol |
| Synonyms | 1-(3-aminophenyl)ethanone |
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Frequently Asked Questions
In a common synthetic route, 3'-aminoacetophenone is converted to 3'-hydroxyacetophenone through a diazotization and hydrolysis process. The 3'-hydroxyacetophenone intermediate is then used as the primary starting material for the subsequent steps that build the final phenylephrine structure. 3'-Aminoacetophenone serves as a key pharmaceutical intermediate in one of the steps to synthesize phenylephrine hydrochloride.
The CAS number of 3′-Aminoacetophenone is 99-03-6.
The molecular formula of 3′-Aminoacetophenone is C8H9NO.
The listed molecular weight of 3′-Aminoacetophenone is 135.16 g/mol.
3′-Aminoacetophenone is listed as being used in connection with the following API: Phenylephrine hydrochloride.
The listed synonym or IUPAC name for 3′-Aminoacetophenone is 1-(3-aminophenyl)ethanone.