1H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-4-[(3-iodopropyl)amino]-

95%

Reagent Code: #223727
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CAS Number 2570254-31-6

science Other reagents with same CAS 2570254-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 441.23 g/mol
Formula C₁₆H₁₆IN₃O₄
thermostat Physical Properties
Boiling Point 647.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.815±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of targeted protein degraders, particularly cereblon E3 ligase modulators. Its structure enables conjugation to other pharmacophores for developing PROTACs (proteolysis-targeting chimeras), which are investigational drugs designed to degrade disease-causing proteins. The iodopropyl group facilitates further chemical modifications through coupling reactions, making it valuable in creating compound libraries for drug discovery. Also employed in biochemical assays to study protein-protein interactions and ubiquitination pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿10,300.00
25mg
10-20 days ฿41,200.00
1H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-4-[(3-iodopropyl)amino]-
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Used in pharmaceutical research as a key intermediate in the synthesis of targeted protein degraders, particularly cereblon E3 ligase modulators. Its structure enables conjugation to other pharmacophores for developing PROTACs (proteolysis-targeting chimeras), which are investigational drugs designed to degrade disease-causing proteins. The iodopropyl group facilitates further chemical modifications through coupling reactions, making it valuable in creating compound libraries for drug discovery. Also emp

Used in pharmaceutical research as a key intermediate in the synthesis of targeted protein degraders, particularly cereblon E3 ligase modulators. Its structure enables conjugation to other pharmacophores for developing PROTACs (proteolysis-targeting chimeras), which are investigational drugs designed to degrade disease-causing proteins. The iodopropyl group facilitates further chemical modifications through coupling reactions, making it valuable in creating compound libraries for drug discovery. Also employed in biochemical assays to study protein-protein interactions and ubiquitination pathways.

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