5-Bromo-6-oxo-1,6-dihydropyridine-3-carbonitrile
≥95%
- Product Code: 120247
CAS:
19840-44-9
| Molecular Weight: | 199.01 g./mol | Molecular Formula: | C₆H₃BrN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11100229 | |
| Melting Point: | Boiling Point: | 345.139°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring both a bromo and a nitrile group, makes it particularly valuable in cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceutical and agrochemical research. Additionally, the oxo group enhances its reactivity, allowing it to participate in various cyclization and functionalization processes. Researchers often employ it in the synthesis of heterocyclic compounds, which are crucial in drug discovery due to their diverse biological activities. Its application extends to the development of potential therapeutic agents, particularly in the design of molecules targeting specific enzymes or receptors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,205.00 |
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| 0.250 | 10-20 days | ฿3,303.00 |
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| 1.000 | 10-20 days | ฿8,226.00 |
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5-Bromo-6-oxo-1,6-dihydropyridine-3-carbonitrile
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring both a bromo and a nitrile group, makes it particularly valuable in cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceutical and agrochemical research. Additionally, the oxo group enhances its reactivity, allowing it to participate in various cyclization and functionalization processes. Researchers often employ it in the synthesis of heterocyclic compounds, which are crucial in drug discovery due to their diverse biological activities. Its application extends to the development of potential therapeutic agents, particularly in the design of molecules targeting specific enzymes or receptors.
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