tert-Butyl 2-(4-bromopyridin-2-yl)acetate
96%
- Product Code: 115745
CAS:
1266119-33-8
Molecular Weight: | 272.14 g./mol | Molecular Formula: | C₁₁H₁₄BrNO₂ |
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EC Number: | MDL Number: | MFCD18447573 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate for the development of more complex molecules. Its structure, featuring a bromopyridine moiety and an ester group, makes it valuable in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine ring into target compounds. Additionally, it serves as a building block in the preparation of ligands for catalysis or materials science applications. Its reactivity and functional groups allow for further modifications, enabling the creation of diverse chemical entities for drug discovery and development.
Product Specification:
Test | Specification |
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Appearance | Liquid |
Purity (%) | 95.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $131.03 |
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0.250 | 10-20 days | $262.90 |
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1.000 | 10-20 days | $655.15 |
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5.000 | 10-20 days | $2,300.63 |
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tert-Butyl 2-(4-bromopyridin-2-yl)acetate
This chemical is primarily used in organic synthesis as a versatile intermediate for the development of more complex molecules. Its structure, featuring a bromopyridine moiety and an ester group, makes it valuable in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine ring into target compounds. Additionally, it serves as a building block in the preparation of ligands for catalysis or materials science applications. Its reactivity and functional groups allow for further modifications, enabling the creation of diverse chemical entities for drug discovery and development.
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