6-Bromoquinoline-2-carbaldehyde
≥95%
- Product Code: 120684
CAS:
98948-91-5
| Molecular Weight: | 236.07 g./mol | Molecular Formula: | C₁₀H₆BrNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06824164 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
6-Bromoquinoline-2-carbaldehyde finds its primary application in organic synthesis, particularly as a versatile intermediate for the preparation of more complex quinoline derivatives. Its aldehyde group allows for further functionalization through reactions such as condensation, reduction, or nucleophilic addition, making it valuable in the development of pharmaceuticals, agrochemicals, and materials science. In medicinal chemistry, it serves as a key building block for the synthesis of compounds with potential biological activities, including antimicrobial, anticancer, and anti-inflammatory agents. Additionally, its bromine substituent enables participation in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, facilitating the creation of diverse heterocyclic structures. This compound is also utilized in the synthesis of fluorescent dyes and ligands for coordination chemistry, contributing to advancements in analytical and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,177.00 |
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| 0.250 | 10-20 days | ฿6,336.00 |
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6-Bromoquinoline-2-carbaldehyde
6-Bromoquinoline-2-carbaldehyde finds its primary application in organic synthesis, particularly as a versatile intermediate for the preparation of more complex quinoline derivatives. Its aldehyde group allows for further functionalization through reactions such as condensation, reduction, or nucleophilic addition, making it valuable in the development of pharmaceuticals, agrochemicals, and materials science. In medicinal chemistry, it serves as a key building block for the synthesis of compounds with potential biological activities, including antimicrobial, anticancer, and anti-inflammatory agents. Additionally, its bromine substituent enables participation in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, facilitating the creation of diverse heterocyclic structures. This compound is also utilized in the synthesis of fluorescent dyes and ligands for coordination chemistry, contributing to advancements in analytical and industrial applications.
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