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N-Acetyl-L-Thioproline丨CAS 5025-82-1 Supplier in China
N-Acetyl-L-Thioproline, CAS 5025-82-1, is a sulfur-containing, N-acetylated proline derivative of interest in organic synthesis and specialized chemical research. Its cyclic structure and sulfur functionality make it a potential intermediate for developing structurally modified amino acid derivatives and other compounds for research applications. Its suitability for a particular synthesis depends on the target molecule, reaction conditions, and verified product specifications.
Chemical Identifiers
| InChI | InChI=1S/C6H9NO3S/c1-4(8)7-3-11-2-5(7)6(9)10/h5H,2-3H2,1H3,(H,9,10) |
| InChI Key | WXTBYSIPOKXCPM-UHFFFAOYSA-N |
| Smiles | CC(=O)N1CSCC1C(=O)O |
| EC No. | 225-713-6 |
| MDL No. | MFCD00070139 |
| PubChem CID | 98928 |
Applications
Pharmaceutical Research and Drug Discovery
Sulfur-containing heterocyclic compounds are explored in medicinal chemistry for their potential contributions to molecular structure and biological activity. N-Acetyl-L-Thioproline may be considered as a research intermediate in the synthesis of related compounds for exploratory pharmaceutical research. Its role in a specific drug discovery program should be established through structure verification and experimental evaluation rather than assumed from its chemical class alone.
Amino Acid Derivative Research
Modified amino acids are valuable research materials for studying how structural changes influence molecular properties and chemical reactivity. N-Acetyl-L-Thioproline may support investigations into N-protected amino acid analogues and related sulfur-containing compounds, including research focused on molecular design and the preparation of specialized intermediates.
Organic Synthesis and Chemical Research
Reaction Development and Mechanistic Studies
Specialized organic compounds can help researchers examine reaction selectivity, functional-group compatibility, and synthetic pathways. N-Acetyl-L-Thioproline may be used in suitable reaction-development studies to investigate transformations of related cyclic amino acid derivatives and sulfur-containing structures, depending on the desired products and experimental conditions.
