tert-Butyl (4-bromopyridin-2-yl)(methyl)carbamate

≥95%

  • Product Code: 126274
  CAS:    946000-13-1
Molecular Weight: 287.15 g./mol Molecular Formula: C11H15BrN2O2
EC Number: MDL Number: MFCD13189516
Melting Point: Boiling Point: 348.769°C at 760 mmHg
Density: Storage Condition: 2-8°C, store in inert gas
Product Description: This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. Its structure, featuring a bromopyridine moiety, makes it a valuable building block for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing heterocyclic frameworks. Additionally, it can serve as a precursor in the design of ligands for catalysis or as a component in the development of agrochemicals. Its stability and reactivity make it a useful tool in medicinal chemistry and drug discovery research.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days £237.03
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0.250 10-20 days £474.50
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tert-Butyl (4-bromopyridin-2-yl)(methyl)carbamate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. Its structure, featuring a bromopyridine moiety, makes it a valuable building block for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing heterocyclic frameworks. Additionally, it can serve as a precursor in the design of ligands for catalysis or as a component in the development of agrochemicals. Its stability and reactivity make it a useful tool in medicinal chemistry and drug discovery research.
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