Methyl 2-(Cbz-amino)-2-(tetrahydrothiopyran-4-ylidene)acetate
≥95%
- Product Code: 58268
CAS:
894790-18-2
| Molecular Weight: | 321.39 g./mol | Molecular Formula: | C₁₆H₁₉NO₄S |
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| EC Number: | MDL Number: | MFCD22574985 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, where its unique structure allows for the incorporation of tetrahydrothiopyran and Cbz-protected amino groups into target molecules. The Cbz (carbobenzyloxy) group acts as a protective moiety for amines, enabling selective reactions in multi-step synthetic processes. Additionally, the tetrahydrothiopyran moiety can contribute to the biological activity of the final compound, making it valuable in drug discovery and medicinal chemistry. Its ester functional group also provides a reactive site for further modifications, such as hydrolysis or reduction, to achieve desired chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $261.12 |
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| 5.000 | 10-20 days | $941.31 |
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Methyl 2-(Cbz-amino)-2-(tetrahydrothiopyran-4-ylidene)acetate
This compound is primarily utilized in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, where its unique structure allows for the incorporation of tetrahydrothiopyran and Cbz-protected amino groups into target molecules. The Cbz (carbobenzyloxy) group acts as a protective moiety for amines, enabling selective reactions in multi-step synthetic processes. Additionally, the tetrahydrothiopyran moiety can contribute to the biological activity of the final compound, making it valuable in drug discovery and medicinal chemistry. Its ester functional group also provides a reactive site for further modifications, such as hydrolysis or reduction, to achieve desired chemical transformations.
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