2-Acetamido-3-(benzylamino)-3-oxopropyl Acetate
| Product Name | 2-Acetamido-3-(benzylamino)-3-oxopropyl Acetate |
|---|---|
| Alternate Names | Lacosamide Impurities, Impurities of Lacosamide |
| CAT No. | CS-O-36045 |
| CAS No. | 1822463-67-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 278.31 g/mol |
| Mol. For. | C14H18N2O4 |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Lacosamide |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
2-Acetamido-3-(benzylamino)-3-oxopropyl Acetate is a chemical compound that is commonly known as ABOPA. This organic compound has a molecular formula of C16H19N3O4 and a molecular weight of 325.34 g/mol. ABOPA is a white to off-white crystalline powder that is soluble in common organic solvents like ethanol and methanol.
ABOPA is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various pharmaceutical compounds. It is commonly used as a starting material for the synthesis of anti-inflammatory and anti-cancer drugs. ABOPA is also used in the preparation of chiral ligands and catalysts.
The chemical structure of ABOPA contains an acetamide group, benzylamino group, and an oxopropyl acetate group. These functional groups make ABOPA a versatile intermediate in the synthesis of various organic compounds. ABOPA is synthesized by the reaction of benzylamine with ethyl acetoacetate, followed by the acetylation of the resulting compound with acetic anhydride.
Overall, ABOPA is an important intermediate in the pharmaceutical industry due to its versatile chemical structure and reactivity. Its unique functional groups make it a valuable starting material for the synthesis of various drugs and organic compounds.
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Related Compounds
O-Acetyl Lacosamide | N-Nitroso Lacosamide | Lacosamide isobutyl carbonate impurity | Lacosamide EP Impurity I | N- (2-acetamino-3-methoxypropionyl) benzoamide | Lacosamide Impurity 15 | Lacosamide Impurity 14 | Desacetyl Desmethyl Lacosamide | Lacosamide chiral impurity | N-desacetyl Lacosamide oxalate salt | Lacosamide (racemate) | Lacosamide N-Methyl Impurity(racemic) | Lacosamide Impurity C | Lacosamide Impurity A | N-Nitroso Lacosamide 1 | Lacosamide Related Compound D (Oxalate Salt) | Lacosamide EP Impurity H | Lacosamide Impurity H(S,S ISOMER) | N-Methyl Lacosamide | Lacosamide Impurity B |