2,4-Dibromopyridine-3-carboxaldehyde

≥98%

Reagent Code: #78156
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CAS Number 128071-91-0

science Other reagents with same CAS 128071-91-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.9 g/mol
Formula C₆H₃Br₂NO
badge Registry Numbers
MDL Number MFCD10574708
thermostat Physical Properties
Boiling Point 313.4ºC
inventory_2 Storage & Handling
Density 2.09 g/cm3
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both bromine atoms and an aldehyde group, makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating biologically active compounds. Additionally, it is used in the synthesis of heterocyclic compounds, which are significant in medicinal chemistry for their potential therapeutic properties. Its applications extend to material science, where it contributes to the development of organic electronic materials and ligands for catalysis.

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Test Parameter Specification
Appearance Off-white to light yellow Solid
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,543.00
inventory 500mg
10-20 days ฿1,215.00
inventory 1g
10-20 days ฿2,034.00

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2,4-Dibromopyridine-3-carboxaldehyde
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This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both bromine atoms and an aldehyde group, makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating biologically active compounds. Additionally, it is used in the synthesis of heterocyclic compounds, which are significant in medicinal chemistry for their potential therapeutic properties. Its applications extend to material science, where it contributes to the development of organic electronic materials and ligands for catalysis.
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