AX03603
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1mg | 98% | in stock | $48.00 | $34.00 | - + | |
5mg | 98% | in stock | $126.00 | $89.00 | - + | |
10mg | 98% | in stock | $229.00 | $161.00 | - + | |
25mg | 98% | in stock | $511.00 | $358.00 | - + | |
50mg | 98% | in stock | $991.00 | $694.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AX03603 |
Chemical Name: | Vh-298 |
CAS Number: | 2097381-85-4 |
Molecular Formula: | C27H33N5O4S |
Molecular Weight: | 523.647 |
MDL Number: | MFCD30742947 |
SMILES: | O[C@@H]1C[C@H](N(C1)C(=O)[C@H](C(C)(C)C)NC(=O)C1(CC1)C#N)C(=O)NCc1ccc(cc1)c1scnc1C |
(2S,4R)-1-[(2S)-2-[(1-cyanocyclopropanecarbonyl)amino]-3,3-dimethylbutanoyl]-4-hydroxy-N-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide is a versatile compound used in chemical synthesis for its unique structural properties and functional groups. This compound is commonly employed as a chiral building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.The (2S,4R) configuration at the center of the molecule provides a specific stereochemical orientation that can be crucial for controlling the outcome of chemical reactions. The presence of a hydroxy group, a thiazole moiety, and a cyanocyclopropane group offers diverse reactivity and allows for the introduction of various functional groups during synthesis.Furthermore, the pyrrolidine core of the compound serves as a key scaffold for constructing complex molecules through sequential reactions. The thiazole and cyanocyclopropane functionalities enable the compound to participate in important bond-forming reactions, making it a valuable tool for building molecular complexity in a controlled manner.In summary, the application of (2S,4R)-1-[(2S)-2-[(1-cyanocyclopropanecarbonyl)amino]-3,3-dimethylbutanoyl]-4-hydroxy-N-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide in chemical synthesis allows for precise control over stereochemistry, functional group manipulation, and scaffold diversity, making it a valuable asset in the toolbox of synthetic chemists.