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
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
Appearance Liquid
Purity (%) 95.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
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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