3-((tert-Butoxycarbonyl)amino)picolinic acid
≥95%
- Product Code: 117476
CAS:
569687-82-7
| Molecular Weight: | 238.24 g./mol | Molecular Formula: | C₁₁H₁₄N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02181061 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a picolinic acid moiety, makes it valuable in peptide synthesis and drug design. The Boc group protects amines during reactions, allowing for selective modifications, while the picolinic acid component can enhance metal chelation properties, useful in creating metalloenzyme inhibitors. Additionally, it is employed in the preparation of compounds targeting neurological disorders and inflammation, leveraging its ability to interact with specific biological pathways. Its versatility also extends to agrochemical research, where it aids in developing new pesticides and herbicides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿5,364.00 |
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| 5.000 | 10-20 days | ฿18,594.00 |
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| 10.000 | 10-20 days | ฿31,563.00 |
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3-((tert-Butoxycarbonyl)amino)picolinic acid
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a picolinic acid moiety, makes it valuable in peptide synthesis and drug design. The Boc group protects amines during reactions, allowing for selective modifications, while the picolinic acid component can enhance metal chelation properties, useful in creating metalloenzyme inhibitors. Additionally, it is employed in the preparation of compounds targeting neurological disorders and inflammation, leveraging its ability to interact with specific biological pathways. Its versatility also extends to agrochemical research, where it aids in developing new pesticides and herbicides.
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