2-[trans-4-(Boc-amino)cyclohexyl]acetonitrile
≥95%
- Product Code: 80794
CAS:
1313279-47-8
| Molecular Weight: | 238.33 g./mol | Molecular Formula: | C₁₃H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD29060206 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is commonly used in organic synthesis, particularly in the preparation of pharmaceutical intermediates. It serves as a key building block in the development of compounds with potential biological activity, especially in the synthesis of peptides and small molecules targeting specific receptors or enzymes. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection during multi-step reactions, making it valuable in complex chemical processes. Its structure, featuring a cyclohexyl ring, contributes to the stability and conformational control of the final molecules, which is crucial in drug design and medicinal chemistry. Additionally, the nitrile group can be further functionalized, enabling the creation of diverse chemical entities for research and therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿10,800.00 |
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| 1.000 | 10-20 days | ฿19,800.00 |
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2-[trans-4-(Boc-amino)cyclohexyl]acetonitrile
This chemical is commonly used in organic synthesis, particularly in the preparation of pharmaceutical intermediates. It serves as a key building block in the development of compounds with potential biological activity, especially in the synthesis of peptides and small molecules targeting specific receptors or enzymes. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection during multi-step reactions, making it valuable in complex chemical processes. Its structure, featuring a cyclohexyl ring, contributes to the stability and conformational control of the final molecules, which is crucial in drug design and medicinal chemistry. Additionally, the nitrile group can be further functionalized, enabling the creation of diverse chemical entities for research and therapeutic applications.
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