tert-Butyl 3-bromo-6-chloropicolinate
97%
- Product Code: 118048
CAS:
1235036-15-3
| Molecular Weight: | 292.56 g./mol | Molecular Formula: | C₁₀H₁₁BrClNO₂ |
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| EC Number: | MDL Number: | MFCD19443279 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
Widely used in pharmaceutical synthesis as an intermediate for developing active pharmaceutical ingredients (APIs). It plays a key role in the construction of complex molecules, particularly in the preparation of picolinate derivatives.
In agrochemical research, it serves as a building block for creating herbicides and pesticides, leveraging its halogenated structure for enhanced reactivity.
Its application extends to organic synthesis, where it is utilized in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig reactions, to form carbon-carbon and carbon-nitrogen bonds.
Additionally, it is employed in material science for the development of specialized organic compounds with potential use in electronic or photonic materials.
Handling requires care due to its reactive nature, ensuring safe and efficient use in industrial and laboratory settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $35.93 |
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| 0.250 | 10-20 days | $59.60 |
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| 1.000 | 10-20 days | $167.38 |
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| 5.000 | 10-20 days | $669.52 |
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tert-Butyl 3-bromo-6-chloropicolinate
Widely used in pharmaceutical synthesis as an intermediate for developing active pharmaceutical ingredients (APIs). It plays a key role in the construction of complex molecules, particularly in the preparation of picolinate derivatives.
In agrochemical research, it serves as a building block for creating herbicides and pesticides, leveraging its halogenated structure for enhanced reactivity.
Its application extends to organic synthesis, where it is utilized in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig reactions, to form carbon-carbon and carbon-nitrogen bonds.
Additionally, it is employed in material science for the development of specialized organic compounds with potential use in electronic or photonic materials.
Handling requires care due to its reactive nature, ensuring safe and efficient use in industrial and laboratory settings.
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