tert-Butyl 3-((3-bromopyridin-2-yl)oxy)azetidine-1-carboxylate

95%

Reagent Code: #44304
fingerprint
CAS Number 1227381-94-3

science Other reagents with same CAS 1227381-94-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.1900 g/mol
Formula C₁₃H₁₇BrN₂O₃
badge Registry Numbers
MDL Number MFCD17012880
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the pharmaceutical industry for the preparation of biologically active compounds, particularly those targeting neurological disorders or as potential drug candidates. The presence of the bromopyridine moiety makes it a valuable building block for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating diverse chemical structures. Additionally, the azetidine ring and tert-butyloxycarbonyl (Boc) protecting group enhance its utility in peptide synthesis and medicinal chemistry, allowing for further functionalization and modification. Its application extends to agrochemical research, where it serves as a precursor for the synthesis of herbicides or pesticides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,916.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl 3-((3-bromopyridin-2-yl)oxy)azetidine-1-carboxylate
No image available
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the pharmaceutical industry for the preparation of biologically active compounds, particularly those targeting neurological disorders or as potential drug candidates. The presence of the bromopyridine moiety makes it a valuable building block for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating diverse chemical structures. Additionally, the azetidine ring and tert-butyloxycarbonyl (Boc) protecting group enhance its utility in peptide synthesis and medicinal chemistry, allowing for further functionalization and modification. Its application extends to agrochemical research, where it serves as a precursor for the synthesis of herbicides or pesticides.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...