tert-Butyl ((1S,3R)-3-aminocyclohexyl)carbamate
≥95%
- Product Code: 112983
CAS:
1298101-47-9
| Molecular Weight: | 214.31 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD24469814 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily used in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an amine and a carbamate group, makes it valuable for constructing biologically active compounds, such as inhibitors or modulators of specific enzymes or receptors. It is often employed in the preparation of peptides or peptidomimetics, where its stereochemistry and functional groups play a critical role in achieving desired biological activity. Additionally, it can be utilized in the development of drugs targeting neurological disorders, cancer, or infectious diseases, owing to its ability to interact with biological targets selectively. Its tert-butyl group also provides stability during synthetic processes, making it a useful building block in organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $159.27 |
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| 0.250 | 10-20 days | $234.38 |
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| 1.000 | 10-20 days | $715.73 |
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tert-Butyl ((1S,3R)-3-aminocyclohexyl)carbamate
This compound is primarily used in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring both an amine and a carbamate group, makes it valuable for constructing biologically active compounds, such as inhibitors or modulators of specific enzymes or receptors. It is often employed in the preparation of peptides or peptidomimetics, where its stereochemistry and functional groups play a critical role in achieving desired biological activity. Additionally, it can be utilized in the development of drugs targeting neurological disorders, cancer, or infectious diseases, owing to its ability to interact with biological targets selectively. Its tert-butyl group also provides stability during synthetic processes, making it a useful building block in organic chemistry.
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