It provides a protected amino group (Boc) and a stereochemically defined hydroxypropionic backbone, which allows for selective amide bond formation at the hydroxy position while maintaining the desired R-configuration. This ensures the final Lacosamide molecule has the correct stereochemistry, which is critical for its biological activity. (R)-2-tert-Butoxycarbonylamino-3-hydroxypropionic acid (Boc-L-serine) is a key chiral intermediate in the synthesis of Lacosamide, an anticonvulsant drug.
(R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acid
| API Name | Lacosamide |
|---|---|
| CAS No | 6368-20-3 |
| Molecular Formula | C8H15NO5 |
| Molecular Weight | 205.21 g/mol |
| Synonyms | (2R)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid |
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Frequently Asked Questions
It provides a protected amino group (Boc) and a stereochemically defined hydroxypropionic backbone, which allows for selective amide bond formation at the hydroxy position while maintaining the desired R-configuration. This ensures the final Lacosamide molecule has the correct stereochemistry, which is critical for its biological activity. (R)-2-tert-Butoxycarbonylamino-3-hydroxypropionic acid (Boc-L-serine) is a key chiral intermediate in the synthesis of Lacosamide, an anticonvulsant drug.
The CAS number of (R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acid is 6368-20-3.
The molecular formula of (R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acid is C8H15NO5.
The listed molecular weight of (R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acid is 205.21 g/mol.
(R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acid is listed as being used in connection with the following API: Lacosamide.
The listed synonym or IUPAC name for (R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acid is (2R)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid.