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| Product | Description | |
|---|---|---|
| N-Acetyl-L-aspartic acid | N-Acetyl-L-aspartic acid can be used as a reactant to synthesize: Protected homoserine γ-lactones by selective reduction and acid-catalyzed cyclization reaction. Racemic amino substituted succinimide derivatives via cyclocondensation reaction. Group: Amino acids. Alternative Names: (2S)-2-Acetamidobutanedioic acid, N-Acetyl-S-aspartic acid. CAS No. 997-55-7. Molecular formula: HO2CCH2CH(NHCOCH3)CO2H. Mole weight: 175.14. Canonical SMILES: CC(=O)N[C@@H](CC(O)=O)C(O)=O. Catalog: ACM997557-1. |  |
| N-Acetyl-L-aspartic acid | N-Acetyl-L-aspartic acid is a derivative of aspartic acid. Uses: Scientific research. Group: Natural products. CAS No. 997-55-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-113524. |  |
| N-α-Acetyl-L-aspartic acid | N-α-Acetyl-L-aspartic acid, a naturally occurring compound, is ubiquitous in mammals' nervous and immune systems. Its vital function in regulating brain activity renders it a promising therapeutic agent for various neurological conditions. This includes Alzheimer's and multiple sclerosis. In addition, it's investigated for potential efficacy against chemotherapy and radiation-caused neurotoxicity. Synonyms: Acetyl-L-aspartic Acid; Acetylaspartic Acid; L-N-Acetylaspartic Acid; N-Acetyl-L-aspartic Acid; N-Acetylaspartic Acid; Ac-Asp-OH; (S)-2-Acetamidosuccinic acid; (S)-2-(acetylamino)butanedioic acid. Grades: ≥98%. CAS No. 997-55-7. Molecular formula: C6H9NO5. Mole weight: 175.14. |  |
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