Ethyl 2-(6-((tert-butoxycarbonyl)amino)pyridin-2-yl)acetate
95%
- Product Code: 51174
CAS:
408365-87-7
| Molecular Weight: | 280.3200 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₄ |
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| EC Number: | MDL Number: | MFCD10698587 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) due to its reactive ester and protected amine functional groups. The tert-butoxycarbonyl (Boc) group provides stability during synthetic processes, allowing for selective deprotection when needed. Its pyridine ring structure contributes to its role in creating compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. The ester group enables further chemical modifications, making it versatile for coupling reactions or transformations into other functional groups like amides or acids. Its application is significant in medicinal chemistry for designing and optimizing drug candidates, especially in the fields of anti-inflammatory, antiviral, or anticancer therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,250.00 |
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Ethyl 2-(6-((tert-butoxycarbonyl)amino)pyridin-2-yl)acetate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) due to its reactive ester and protected amine functional groups. The tert-butoxycarbonyl (Boc) group provides stability during synthetic processes, allowing for selective deprotection when needed. Its pyridine ring structure contributes to its role in creating compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. The ester group enables further chemical modifications, making it versatile for coupling reactions or transformations into other functional groups like amides or acids. Its application is significant in medicinal chemistry for designing and optimizing drug candidates, especially in the fields of anti-inflammatory, antiviral, or anticancer therapies.
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