It provides the 4‑methoxyphenethylamine backbone required for building the side chain of the drug. During synthesis, this intermediate undergoes further functional group transformations such as hydroxylation, ether formation, and substitution reactions, which convert the phenethylamine structure into the final β₂‑adrenergic agonist framework present in Formoterol. 4‑Methoxy‑N‑ethylamphetamine serves as a phenethylamine intermediate in the synthesis of Formoterol.
4-methoxy-N-ethylamphetamine
| API Name | Formoterol |
|---|---|
| CAS No | 14367-46-5 |
| Molecular Formula | C12H19NO |
| Molecular Weight | 193.28 g/mol |
| Synonyms | N-ethyl-1-(4-methoxyphenyl)propan-2-amine |
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Frequently Asked Questions
It provides the 4‑methoxyphenethylamine backbone required for building the side chain of the drug. During synthesis, this intermediate undergoes further functional group transformations such as hydroxylation, ether formation, and substitution reactions, which convert the phenethylamine structure into the final β₂‑adrenergic agonist framework present in Formoterol. 4‑Methoxy‑N‑ethylamphetamine serves as a phenethylamine intermediate in the synthesis of Formoterol.
The CAS number of 4-methoxy-N-ethylamphetamine is 14367-46-5.
The molecular formula of 4-methoxy-N-ethylamphetamine is C12H19NO.
The listed molecular weight of 4-methoxy-N-ethylamphetamine is 193.28 g/mol.
4-methoxy-N-ethylamphetamine is listed as being used in connection with the following API: Formoterol.
The listed synonym or IUPAC name for 4-methoxy-N-ethylamphetamine is N-ethyl-1-(4-methoxyphenyl)propan-2-amine.