N-(5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide
98%
- Product Code: 53989
CAS:
1142943-96-1
| Molecular Weight: | 281.1100 g./mol | Molecular Formula: | C₁₀H₉BrN₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28502349 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It plays a significant role in the development of potential therapeutic agents, particularly those targeting enzyme inhibition or receptor modulation. Researchers often employ it in the design and optimization of drug candidates, especially for conditions involving inflammation, cancer, or neurological disorders. Its unique structure allows for the exploration of novel chemical spaces, contributing to the discovery of compounds with enhanced efficacy and selectivity. Additionally, it is used in academic and industrial research to study structure-activity relationships and to develop new methodologies in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £11.81 |
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N-(5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It plays a significant role in the development of potential therapeutic agents, particularly those targeting enzyme inhibition or receptor modulation. Researchers often employ it in the design and optimization of drug candidates, especially for conditions involving inflammation, cancer, or neurological disorders. Its unique structure allows for the exploration of novel chemical spaces, contributing to the discovery of compounds with enhanced efficacy and selectivity. Additionally, it is used in academic and industrial research to study structure-activity relationships and to develop new methodologies in organic synthesis.
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