6-Iodoindoline-2,3-dione

≥95%

Reagent Code: #200276
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CAS Number 20780-77-2

science Other reagents with same CAS 20780-77-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.03 g/mol
Formula C₈H₄INO₂
badge Registry Numbers
MDL Number MFCD01925283
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceutically active compounds. It serves as a key building block in the development of indole-based derivatives, which are common structures in many bioactive molecules and drug candidates. Its iodo functionality allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries. Additionally, it has been explored in the synthesis of fluorescent probes and heterocyclic compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,010.00
inventory 250mg
10-20 days ฿4,210.00

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6-Iodoindoline-2,3-dione
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Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceutically active compounds. It serves as a key building block in the development of indole-based derivatives, which are common structures in many bioactive molecules and drug candidates. Its iodo functionality allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries. Additionally, it has been explored in the synthes

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceutically active compounds. It serves as a key building block in the development of indole-based derivatives, which are common structures in many bioactive molecules and drug candidates. Its iodo functionality allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries. Additionally, it has been explored in the synthesis of fluorescent probes and heterocyclic compounds with potential biological activity.

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