tert-butyl N-[trans-4-[(methanesulfonyloxy)methyl]cyclohexyl]carbamate
98%
- Product Code: 87792
CAS:
683269-95-6
| Molecular Weight: | 307.41 g./mol | Molecular Formula: | C₁₃H₂₅NO₅S |
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| EC Number: | MDL Number: | MFCD28383641 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds targeting neurological and cardiovascular disorders. The presence of the methanesulfonyloxy group makes it a versatile reagent for further functionalization, enabling the introduction of various substituents into the cyclohexyl ring. Additionally, its tert-butyl carbamate moiety provides protection for amine groups during multi-step synthetic processes, ensuring selective reactivity in subsequent reactions. This compound is also valuable in the production of peptidomimetics and other bioactive molecules, where its structural features contribute to enhanced stability and bioavailability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,368.00 |
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| 1.000 | 10-20 days | ฿3,681.00 |
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| 5.000 | 10-20 days | ฿12,861.00 |
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tert-butyl N-[trans-4-[(methanesulfonyloxy)methyl]cyclohexyl]carbamate
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds targeting neurological and cardiovascular disorders. The presence of the methanesulfonyloxy group makes it a versatile reagent for further functionalization, enabling the introduction of various substituents into the cyclohexyl ring. Additionally, its tert-butyl carbamate moiety provides protection for amine groups during multi-step synthetic processes, ensuring selective reactivity in subsequent reactions. This compound is also valuable in the production of peptidomimetics and other bioactive molecules, where its structural features contribute to enhanced stability and bioavailability.
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