3-Bromo-6-chloro-1H-pyrazolo[3,4-d]pyrimidine
≥95%
- Product Code: 118040
CAS:
944903-06-4
| Molecular Weight: | 233.45 g./mol | Molecular Formula: | C₅H₂BrClN₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10697158 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for targeting specific enzymes involved in diseases such as cancer and inflammatory disorders. Researchers often employ it to create novel therapeutic agents due to its ability to interact with diverse biological targets. Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are widely explored for their potential in drug discovery and development. Its application extends to the optimization of drug candidates, enhancing their efficacy and selectivity in preclinical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,147.00 |
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| 0.250 | 10-20 days | ฿10,494.00 |
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| 1.000 | 10-20 days | ฿22,329.00 |
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3-Bromo-6-chloro-1H-pyrazolo[3,4-d]pyrimidine
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for targeting specific enzymes involved in diseases such as cancer and inflammatory disorders. Researchers often employ it to create novel therapeutic agents due to its ability to interact with diverse biological targets. Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are widely explored for their potential in drug discovery and development. Its application extends to the optimization of drug candidates, enhancing their efficacy and selectivity in preclinical studies.
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