6-Bromopyrazolo[1,5-a]pyrimidine-3-carbonitrile
98%
- Product Code: 81536
CAS:
352637-44-6
| Molecular Weight: | 223.03 g./mol | Molecular Formula: | C₇H₃BrN₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00461392 | |
| Melting Point: | 154-156℃ | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development due to its structural properties, which make it a valuable intermediate in the synthesis of various biologically active molecules. It is often employed in the creation of kinase inhibitors, which are crucial in targeting specific pathways involved in diseases such as cancer and inflammatory disorders. Additionally, its pyrazolo[1,5-a]pyrimidine core is a key scaffold in medicinal chemistry, enabling the design of compounds with potential therapeutic applications. Researchers also explore its use in developing agrochemicals, where it may contribute to the formulation of novel pesticides or herbicides. Its versatility in chemical reactions further enhances its utility in organic synthesis, particularly in constructing complex heterocyclic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿5,355.00 |
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| 5.000 | 10-20 days | ฿18,801.00 |
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6-Bromopyrazolo[1,5-a]pyrimidine-3-carbonitrile
This compound is primarily utilized in pharmaceutical research and development due to its structural properties, which make it a valuable intermediate in the synthesis of various biologically active molecules. It is often employed in the creation of kinase inhibitors, which are crucial in targeting specific pathways involved in diseases such as cancer and inflammatory disorders. Additionally, its pyrazolo[1,5-a]pyrimidine core is a key scaffold in medicinal chemistry, enabling the design of compounds with potential therapeutic applications. Researchers also explore its use in developing agrochemicals, where it may contribute to the formulation of novel pesticides or herbicides. Its versatility in chemical reactions further enhances its utility in organic synthesis, particularly in constructing complex heterocyclic compounds.
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