Ethyl 5-bromo-6-methylnicotinate
97%
- Product Code: 120213
CAS:
1190862-70-4
| Molecular Weight: | 244.09 g./mol | Molecular Formula: | C₉H₁₀BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19440560 | |
| Melting Point: | Boiling Point: | 270.5±35.0°C at 3 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both a bromo and a methyl group on the pyridine ring, allows for selective functionalization, making it useful in the design of molecules with specific biological activities. Additionally, it finds application in the development of agrochemicals, where it contributes to the creation of compounds with potential pesticidal or herbicidal properties. Its ester group also enables further chemical modifications, expanding its utility in diverse synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,312.00 |
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| 0.250 | 10-20 days | ฿5,274.00 |
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| 1.000 | 10-20 days | ฿13,212.00 |
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Ethyl 5-bromo-6-methylnicotinate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both a bromo and a methyl group on the pyridine ring, allows for selective functionalization, making it useful in the design of molecules with specific biological activities. Additionally, it finds application in the development of agrochemicals, where it contributes to the creation of compounds with potential pesticidal or herbicidal properties. Its ester group also enables further chemical modifications, expanding its utility in diverse synthetic pathways.
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