5-Methoxy-2-oxoindoline-3-carbaldehyde

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Reagent Code: #207075
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CAS Number 52508-88-0

science Other reagents with same CAS 52508-88-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.18 g/mol
Formula C₁₀H₉NO₃
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MDL Number MFCD08691731
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. It serves as a building block in the preparation of indole-based compounds with potential antidepressant, anxiolytic, or antipsychotic activity. Also employed in the production of dyes and fluorescent probes due to its conjugated aldehyde structure, which allows for easy functionalization and chromophore formation. Its reactivity makes it valuable in multicomponent reactions for generating diverse heterocyclic libraries in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,220.00
inventory 1g
10-20 days ฿2,930.00

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5-Methoxy-2-oxoindoline-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. It serves as a building block in the preparation of indole-based compounds with potential antidepressant, anxiolytic, or antipsychotic activity. Also employed in the production of dyes and fluorescent probes due to its conjugated aldehyde structure, which allows for easy functionalization and chromophore formation. Its reactivity makes i

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. It serves as a building block in the preparation of indole-based compounds with potential antidepressant, anxiolytic, or antipsychotic activity. Also employed in the production of dyes and fluorescent probes due to its conjugated aldehyde structure, which allows for easy functionalization and chromophore formation. Its reactivity makes it valuable in multicomponent reactions for generating diverse heterocyclic libraries in drug discovery.

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