1H-Indole-3-carboxaldehyde Oxime

≥98%

Reagent Code: #195181
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CAS Number 2592-05-4

science Other reagents with same CAS 2592-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.18 g/mol
Formula C₉H₈N₂O
badge Registry Numbers
MDL Number MFCD00022737
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of indole-based compounds with biological activity. Serves as a key building block in agrochemicals for creating plant growth regulators and certain pesticide formulations. Employed in research settings to modify indole structures for studying receptor binding, especially in serotonin and melatonin analogs. Also utilized in the preparation of fluorescent probes for biochemical imaging due to its conjugated structure that supports light absorption and emission. Shows potential in coordination chemistry as a ligand for metal ions in catalytic systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,990.00
inventory 250mg
10-20 days ฿3,300.00
inventory 1g
10-20 days ฿6,470.00

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1H-Indole-3-carboxaldehyde Oxime
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of indole-based compounds with biological activity. Serves as a key building block in agrochemicals for creating plant growth regulators and certain pesticide formulations. Employed in research settings to modify indole structures for studying receptor binding, especially in serotonin and melatonin analogs. Also utilized in the preparation of fluorescent probes for biochemical imaging due to its conjugated structure th

Used in the synthesis of pharmaceutical intermediates, particularly in the development of indole-based compounds with biological activity. Serves as a key building block in agrochemicals for creating plant growth regulators and certain pesticide formulations. Employed in research settings to modify indole structures for studying receptor binding, especially in serotonin and melatonin analogs. Also utilized in the preparation of fluorescent probes for biochemical imaging due to its conjugated structure that supports light absorption and emission. Shows potential in coordination chemistry as a ligand for metal ions in catalytic systems.

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