5-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde
≥95%
- Product Code: 120228
CAS:
878197-68-3
| Molecular Weight: | 225.04 g./mol | Molecular Formula: | C₈H₅BrN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11226918 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,287.00 |
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| 0.250 | 10-20 days | ฿2,070.00 |
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| 1.000 | 10-20 days | ฿5,328.00 |
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| 5.000 | 10-20 days | ฿20,340.00 |
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5-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde
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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