2-Bromo-1,7-naphthyridine
97%
- Product Code: 116614
CAS:
54920-83-1
| Molecular Weight: | 209.04 g./mol | Molecular Formula: | C₈H₅BrN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02181611 | |
| Melting Point: | Boiling Point: | 324.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
2-Bromo-1,7-naphthyridine is primarily utilized in organic synthesis as a versatile building block for the creation of more complex chemical structures. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. Its bromine atom makes it a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the construction of diverse naphthyridine derivatives. These derivatives are often explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory effects. Additionally, it is used in materials science for the design of organic semiconductors and luminescent materials due to its aromatic structure and electron-rich properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,840.00 |
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| 0.250 | 10-20 days | ฿23,650.00 |
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| 1.000 | 10-20 days | ฿48,920.00 |
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2-Bromo-1,7-naphthyridine
2-Bromo-1,7-naphthyridine is primarily utilized in organic synthesis as a versatile building block for the creation of more complex chemical structures. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. Its bromine atom makes it a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the construction of diverse naphthyridine derivatives. These derivatives are often explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory effects. Additionally, it is used in materials science for the design of organic semiconductors and luminescent materials due to its aromatic structure and electron-rich properties.
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