Methyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate
95%
- Product Code: 118084
CAS:
1823420-32-1
| Molecular Weight: | 256.06 g./mol | Molecular Formula: | C₈H₆BrN₃O₂ |
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| EC Number: | MDL Number: | MFCD28346180 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the synthesis of pharmaceutical agents, where its structure serves as a building block for active pharmaceutical ingredients (APIs). The bromine atom and ester functional group present in the molecule make it highly reactive, enabling it to participate in various coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for constructing drug-like molecules. Additionally, its pyrazolo[1,5-a]pyrimidine core is of interest in medicinal chemistry due to its potential biological activity, making it a candidate for the development of compounds targeting specific enzymes or receptors. Researchers also explore its use in the creation of agrochemicals, where its structural features could contribute to the design of novel pesticides or herbicides. Overall, its versatility in synthetic chemistry makes it a valuable tool for drug discovery and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,743.00 |
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| 0.250 | 10-20 days | ฿8,064.00 |
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Methyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the synthesis of pharmaceutical agents, where its structure serves as a building block for active pharmaceutical ingredients (APIs). The bromine atom and ester functional group present in the molecule make it highly reactive, enabling it to participate in various coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for constructing drug-like molecules. Additionally, its pyrazolo[1,5-a]pyrimidine core is of interest in medicinal chemistry due to its potential biological activity, making it a candidate for the development of compounds targeting specific enzymes or receptors. Researchers also explore its use in the creation of agrochemicals, where its structural features could contribute to the design of novel pesticides or herbicides. Overall, its versatility in synthetic chemistry makes it a valuable tool for drug discovery and material science applications.
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