2-Bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid
≥95%
- Product Code: 116732
CAS:
1422772-78-8
| Molecular Weight: | 242.03 g./mol | Molecular Formula: | C₇H₄BrN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26793713 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly as a key intermediate in the synthesis of biologically active molecules. Its unique structure makes it valuable for designing and producing compounds with potential therapeutic applications, especially in the field of oncology. Researchers leverage its reactivity to create novel drug candidates targeting specific enzymes or receptors involved in disease pathways. Additionally, it serves as a building block in medicinal chemistry for the development of small-molecule inhibitors and other pharmacologically active agents. Its application is also explored in the study of biochemical interactions and the optimization of drug-like properties for enhanced efficacy and safety.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,361.00 |
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| 0.250 | 10-20 days | ฿13,410.00 |
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| 1.000 | 10-20 days | ฿33,606.00 |
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2-Bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid
This compound is primarily utilized in pharmaceutical research and development, particularly as a key intermediate in the synthesis of biologically active molecules. Its unique structure makes it valuable for designing and producing compounds with potential therapeutic applications, especially in the field of oncology. Researchers leverage its reactivity to create novel drug candidates targeting specific enzymes or receptors involved in disease pathways. Additionally, it serves as a building block in medicinal chemistry for the development of small-molecule inhibitors and other pharmacologically active agents. Its application is also explored in the study of biochemical interactions and the optimization of drug-like properties for enhanced efficacy and safety.
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