Ethyl 7-bromoimidazo[1,5-a]pyridine-1-carboxylate
≥95%
- Product Code: 120895
CAS:
1363381-07-0
| Molecular Weight: | 269.10 g./mol | Molecular Formula: | C₁₀H₉BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD18074243 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
Ethyl 7-bromoimidazo[1,5-a]pyridine-1-carboxylate is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of various pharmaceutical compounds. Its unique structure makes it valuable for constructing complex molecules, particularly those targeting neurological and inflammatory disorders. Researchers often employ it in the synthesis of imidazo[1,5-a]pyridine derivatives, which are known for their potential therapeutic applications, including as anxiolytics and anticonvulsants. Additionally, its bromo-substituted aromatic ring allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. This compound is also explored in material science for designing organic electronic materials due to its conjugated system and potential for charge transport.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,728.00 |
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| 0.250 | 10-20 days | ฿21,465.00 |
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| 1.000 | 10-20 days | ฿53,667.00 |
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Ethyl 7-bromoimidazo[1,5-a]pyridine-1-carboxylate
Ethyl 7-bromoimidazo[1,5-a]pyridine-1-carboxylate is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of various pharmaceutical compounds. Its unique structure makes it valuable for constructing complex molecules, particularly those targeting neurological and inflammatory disorders. Researchers often employ it in the synthesis of imidazo[1,5-a]pyridine derivatives, which are known for their potential therapeutic applications, including as anxiolytics and anticonvulsants. Additionally, its bromo-substituted aromatic ring allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. This compound is also explored in material science for designing organic electronic materials due to its conjugated system and potential for charge transport.
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