2-(But-3-yn-1-yl)isoindoline-1,3-dione
97%
- Product Code: 71210
CAS:
14396-90-8
| Molecular Weight: | 199.21 g./mol | Molecular Formula: | C₁₂H₉NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03695464 | |
| Melting Point: | 137-142 °C (lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its structure, featuring an isoindoline-1,3-dione core and a terminal alkyne, makes it suitable for click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition (CuAAC). This reaction is widely employed in drug discovery, materials science, and bioconjugation, where it helps in linking molecules efficiently and selectively. Additionally, the compound can be used in the development of pharmaceutical intermediates, agrochemicals, and functional materials due to its reactive alkyne group, which allows for further functionalization. Its applications also extend to polymer chemistry, where it can serve as a monomer or crosslinking agent to modify polymer properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $39.15 |
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| 1.000 | 10-20 days | $85.06 |
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| 5.000 | 10-20 days | $297.03 |
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2-(But-3-yn-1-yl)isoindoline-1,3-dione
This compound is primarily utilized in organic synthesis as a versatile building block for the creation of more complex molecules. Its structure, featuring an isoindoline-1,3-dione core and a terminal alkyne, makes it suitable for click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition (CuAAC). This reaction is widely employed in drug discovery, materials science, and bioconjugation, where it helps in linking molecules efficiently and selectively. Additionally, the compound can be used in the development of pharmaceutical intermediates, agrochemicals, and functional materials due to its reactive alkyne group, which allows for further functionalization. Its applications also extend to polymer chemistry, where it can serve as a monomer or crosslinking agent to modify polymer properties.
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