6-Ethynylpyridin-3-amine
97%
- Product Code: 50024
CAS:
1256824-94-8
| Molecular Weight: | 118.14 g./mol | Molecular Formula: | C₇H₆N₂ |
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| EC Number: | MDL Number: | MFCD18256370 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
6-Ethynylpyridin-3-amine is primarily utilized in the field of organic synthesis and pharmaceutical research. Its structure, featuring both an ethynyl group and an amine group, makes it a valuable building block for the development of complex molecules. It is often employed in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole derivatives, which are important in drug discovery and material science. Additionally, this compound serves as an intermediate in the synthesis of various biologically active compounds, including potential therapeutic agents targeting neurological disorders, cancer, and infectious diseases. Its versatility also extends to the development of fluorescent probes and molecular sensors, aiding in biochemical studies and diagnostics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $169.31 |
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| 0.250 | 10-20 days | $296.49 |
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| 1.000 | 10-20 days | $741.22 |
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6-Ethynylpyridin-3-amine
6-Ethynylpyridin-3-amine is primarily utilized in the field of organic synthesis and pharmaceutical research. Its structure, featuring both an ethynyl group and an amine group, makes it a valuable building block for the development of complex molecules. It is often employed in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole derivatives, which are important in drug discovery and material science. Additionally, this compound serves as an intermediate in the synthesis of various biologically active compounds, including potential therapeutic agents targeting neurological disorders, cancer, and infectious diseases. Its versatility also extends to the development of fluorescent probes and molecular sensors, aiding in biochemical studies and diagnostics.
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