Methyl 5-bromo-4-methylpyrimidine-2-carboxylate
95%
- Product Code: 61399
CAS:
1823969-59-0
| Molecular Weight: | 231.04668 g./mol | Molecular Formula: | C₇H₇BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD26517001 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Methyl 5-bromo-4-methylpyrimidine-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of various active pharmaceutical ingredients (APIs). Specifically, it is utilized in the preparation of pyrimidine derivatives, which are often explored for their potential therapeutic properties, such as antiviral, anticancer, or anti-inflammatory activities. Additionally, this compound is employed in research settings to study reaction mechanisms and to develop novel synthetic pathways for heterocyclic compounds. Its bromo and ester functional groups make it a versatile reagent for further chemical modifications, including cross-coupling reactions and nucleophilic substitutions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿4,662.00 |
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| 0.050 | 10-20 days | ฿14,292.00 |
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| 0.250 | 10-20 days | ฿43,200.00 |
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Methyl 5-bromo-4-methylpyrimidine-2-carboxylate
Methyl 5-bromo-4-methylpyrimidine-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of various active pharmaceutical ingredients (APIs). Specifically, it is utilized in the preparation of pyrimidine derivatives, which are often explored for their potential therapeutic properties, such as antiviral, anticancer, or anti-inflammatory activities. Additionally, this compound is employed in research settings to study reaction mechanisms and to develop novel synthetic pathways for heterocyclic compounds. Its bromo and ester functional groups make it a versatile reagent for further chemical modifications, including cross-coupling reactions and nucleophilic substitutions.
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