5-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde

≥95%

Reagent Code: #120228
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CAS Number 878197-68-3

science Other reagents with same CAS 878197-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.04 g/mol
Formula C₈H₅BrN₂O
badge Registry Numbers
MDL Number MFCD11226918
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo group and an aldehyde functional group, makes it particularly valuable in cross-coupling reactions, which are essential for constructing diverse heterocyclic compounds. These heterocycles are often explored for their potential pharmacological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, the compound is employed in the synthesis of fluorescent dyes and sensors, leveraging its imidazopyridine core for applications in bioimaging and molecular detection. Its versatility also extends to material science, where it contributes to the creation of organic electronic materials and optoelectronic devices.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,287.00
inventory 250mg
10-20 days ฿2,070.00
inventory 1g
10-20 days ฿5,328.00
inventory 5g
10-20 days ฿20,340.00
5-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo group and an aldehyde functional group, makes it particularly valuable in cross-coupling reactions, which are essential for constructing diverse heterocyclic compounds. These heterocycles are often explored for their potential pharmacological activities, including antimicrobial, anticancer, and anti-inflammatory p

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo group and an aldehyde functional group, makes it particularly valuable in cross-coupling reactions, which are essential for constructing diverse heterocyclic compounds. These heterocycles are often explored for their potential pharmacological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, the compound is employed in the synthesis of fluorescent dyes and sensors, leveraging its imidazopyridine core for applications in bioimaging and molecular detection. Its versatility also extends to material science, where it contributes to the creation of organic electronic materials and optoelectronic devices.

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