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

≥95%

Reagent Code: #126274
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CAS Number 946000-13-1

science Other reagents with same CAS 946000-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.15 g/mol
Formula C11H15BrN2O2
badge Registry Numbers
MDL Number MFCD13189516
thermostat Physical Properties
Boiling Point 348.769°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store in inert gas

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,980.00
inventory 100mg
10-20 days ฿10,480.00

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

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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