Ethyl 3-bromo-4,5,6,7-tetrahydro-[1,2,3]triazolo[1,5-a]pyridine-6-carboxylate
95%
- Product Code: 65114
CAS:
1273565-10-8
| Molecular Weight: | 274.11 g./mol | Molecular Formula: | C₉H₁₂BrN₃O₂ |
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| EC Number: | MDL Number: | MFCD18792955 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique triazolo-pyridine core makes it valuable in the construction of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers employ it in the synthesis of molecules that may exhibit biological properties, such as antimicrobial, anti-inflammatory, or anticancer effects. Additionally, its ethyl ester group allows for further functionalization, enabling the creation of diverse derivatives for drug discovery and medicinal chemistry studies. The bromo substituent also provides a reactive site for cross-coupling reactions, facilitating the formation of carbon-carbon bonds in the synthesis of advanced organic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £585.21 |
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Ethyl 3-bromo-4,5,6,7-tetrahydro-[1,2,3]triazolo[1,5-a]pyridine-6-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique triazolo-pyridine core makes it valuable in the construction of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers employ it in the synthesis of molecules that may exhibit biological properties, such as antimicrobial, anti-inflammatory, or anticancer effects. Additionally, its ethyl ester group allows for further functionalization, enabling the creation of diverse derivatives for drug discovery and medicinal chemistry studies. The bromo substituent also provides a reactive site for cross-coupling reactions, facilitating the formation of carbon-carbon bonds in the synthesis of advanced organic materials.
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