4-Iodoindoline-2,3-dione
98%
- Product Code: 200444
CAS:
20780-75-0
| Molecular Weight: | 273.03 g./mol | Molecular Formula: | C₈H₄INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427300 | |
| Melting Point: | 227-229 °C (lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, inert gas, light-proof |
Product Description:
Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and bioactive compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in reactions involving palladium-catalyzed coupling due to the presence of the iodo group, enabling the formation of carbon-carbon bonds. Also explored in the synthesis of indole-based derivatives with potential antimicrobial, antitumor, and anti-inflammatory activities. Its reactivity supports use in medicinal chemistry research for designing kinase inhibitors and other enzyme modulators.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1g | 10-20 days | $48.41 |
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| 5g | 10-20 days | $198.56 |
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| 25g | 10-20 days | $642.23 |
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4-Iodoindoline-2,3-dione
Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and bioactive compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in reactions involving palladium-catalyzed coupling due to the presence of the iodo group, enabling the formation of carbon-carbon bonds. Also explored in the synthesis of indole-based derivatives with potential antimicrobial, antitumor, and anti-inflammatory activities. Its reactivity supports use in medicinal chemistry research for designing kinase inhibitors and other enzyme modulators.
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