2-(3-Iodopropyl)isoindoline-1,3-dione
97%
- Product Code: 200491
CAS:
5457-29-4
| Molecular Weight: | 315.11 g./mol | Molecular Formula: | C₁₁H₁₀INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00458300 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, avoid light, inert gas storage |
Product Description:
Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized isoindoline derivatives, which are valuable in pharmaceutical and agrochemical research. Its iodine functionality allows for further transformations via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. It is also employed in the development of bioactive compounds and functional materials where the isoindoline scaffold plays a key structural role. The reactivity of the alkyl iodide group makes it suitable for nucleophilic substitution, facilitating the introduction of the isoindoline moiety into larger molecular architectures.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $96.81 |
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| 1.000 | 10-20 days | $264.63 |
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| 5.000 | 10-20 days | $1,146.61 |
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2-(3-Iodopropyl)isoindoline-1,3-dione
Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized isoindoline derivatives, which are valuable in pharmaceutical and agrochemical research. Its iodine functionality allows for further transformations via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. It is also employed in the development of bioactive compounds and functional materials where the isoindoline scaffold plays a key structural role. The reactivity of the alkyl iodide group makes it suitable for nucleophilic substitution, facilitating the introduction of the isoindoline moiety into larger molecular architectures.
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