1-Phenethylindoline-2,3-dione

98%

Reagent Code: #223083
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CAS Number 41042-17-5

science Other reagents with same CAS 41042-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.28 g/mol
Formula C₁₆H₁₃NO₂
badge Registry Numbers
MDL Number MFCD00224229
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in organic synthesis as a key intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry, particularly in the creation of serotonin receptor modulators and anti-inflammatory agents. Also employed in research settings to study reaction mechanisms involving diketones and heterocyclic ring systems. Shows potential in the design of kinase inhibitors due to its ability to interact with enzyme active sites. Limited use in industrial applications; mainly confined to laboratory-scale synthesis and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,550.00
inventory 250mg
10-20 days ฿17,930.00
inventory 1g
10-20 days ฿48,400.00

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1-Phenethylindoline-2,3-dione
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Used primarily in organic synthesis as a key intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry, particularly in the creation of serotonin receptor modulators and anti-inflammatory agents. Also employed in research settings to study reaction mechanisms involving diketones and heterocyclic ring systems. Shows potential in the design of kinase inhibitors due to its ability to interact with enz

Used primarily in organic synthesis as a key intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives, which are common in medicinal chemistry, particularly in the creation of serotonin receptor modulators and anti-inflammatory agents. Also employed in research settings to study reaction mechanisms involving diketones and heterocyclic ring systems. Shows potential in the design of kinase inhibitors due to its ability to interact with enzyme active sites. Limited use in industrial applications; mainly confined to laboratory-scale synthesis and drug discovery.

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