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AX03603

2097381-85-4 | Vh-298

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.

Description
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

 

Upstream Synthesis Route
  • (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.
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