tert-butyl (cis-4-hydroxycyclohexyl)carbamate
95%
- Product Code: 58648
CAS:
167081-25-6
| Molecular Weight: | 215.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 337.7°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as an intermediate in the production of various bioactive compounds and drug candidates. Its structure, featuring both a tert-butyl group and a cyclohexyl moiety, makes it valuable for developing molecules with specific stereochemistry and stability. It is often employed in the synthesis of enzyme inhibitors, receptor modulators, and other therapeutic agents targeting neurological and metabolic disorders. Additionally, its hydroxyl and carbamate functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for research and development purposes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Slightly pale reddish yellow : Crystal - Powder |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $12.04 |
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| 1.000 | 10-20 days | $26.99 |
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| 5.000 | 10-20 days | $77.66 |
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| 25.000 | 10-20 days | $206.81 |
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tert-butyl (cis-4-hydroxycyclohexyl)carbamate
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as an intermediate in the production of various bioactive compounds and drug candidates. Its structure, featuring both a tert-butyl group and a cyclohexyl moiety, makes it valuable for developing molecules with specific stereochemistry and stability. It is often employed in the synthesis of enzyme inhibitors, receptor modulators, and other therapeutic agents targeting neurological and metabolic disorders. Additionally, its hydroxyl and carbamate functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for research and development purposes.
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