methyl4-bromo-6-((tert-butoxycarbonyl)amino)picolinate
≥95%
- Product Code: 87755
CAS:
885326-87-4
| Molecular Weight: | 331.16 g./mol | Molecular Formula: | C₁₂H₁₅BrN₂O₄ |
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| EC Number: | MDL Number: | MFCD11226180 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the preparation of complex molecules, especially those involving picolinate derivatives. Its bromo and tert-butoxycarbonyl (Boc) protected amino groups make it a versatile building block for constructing more elaborate structures. The Boc group allows for selective deprotection, enabling further functionalization, while the bromo substituent facilitates cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in drug discovery. Additionally, its picolinate moiety is often utilized in chelating agents or metal coordination studies, making it valuable in materials science and catalysis research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿42,327.00 |
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methyl4-bromo-6-((tert-butoxycarbonyl)amino)picolinate
This chemical is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the preparation of complex molecules, especially those involving picolinate derivatives. Its bromo and tert-butoxycarbonyl (Boc) protected amino groups make it a versatile building block for constructing more elaborate structures. The Boc group allows for selective deprotection, enabling further functionalization, while the bromo substituent facilitates cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in drug discovery. Additionally, its picolinate moiety is often utilized in chelating agents or metal coordination studies, making it valuable in materials science and catalysis research.
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