Benzyl (trans-4-aminocyclohexyl)carbamate
95%
- Product Code: 71742
CAS:
149423-77-8
| Molecular Weight: | 248.32 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 409.5°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various therapeutic agents. Its structure is particularly valuable in the production of drugs targeting neurological disorders, where the trans-4-aminocyclohexyl moiety plays a crucial role in binding to specific receptors in the brain. Additionally, it is employed in the creation of enzyme inhibitors, which are essential in treating conditions like cancer and autoimmune diseases. The benzyl group enhances the compound's stability and bioavailability, making it a preferred choice in medicinal chemistry. Furthermore, it is explored in the development of novel analgesics and anti-inflammatory medications, leveraging its ability to modulate pain pathways effectively.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white solid |
| 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 | ฿2,850.00 |
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| 1.000 | 10-20 days | ฿6,890.00 |
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Benzyl (trans-4-aminocyclohexyl)carbamate
Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various therapeutic agents. Its structure is particularly valuable in the production of drugs targeting neurological disorders, where the trans-4-aminocyclohexyl moiety plays a crucial role in binding to specific receptors in the brain. Additionally, it is employed in the creation of enzyme inhibitors, which are essential in treating conditions like cancer and autoimmune diseases. The benzyl group enhances the compound's stability and bioavailability, making it a preferred choice in medicinal chemistry. Furthermore, it is explored in the development of novel analgesics and anti-inflammatory medications, leveraging its ability to modulate pain pathways effectively.
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