4-Methyl-5-nitro-1H-indole

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Reagent Code: #206747
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CAS Number 165250-69-1

science Other reagents with same CAS 165250-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.17 g/mol
Formula C₉H₈N₂O₂
thermostat Physical Properties
Boiling Point 359.9°C
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 drug candidates targeting inflammatory and neurological disorders. Serves as a building block in agrochemicals for creating novel pesticides with improved efficacy. Employed in research settings to explore nitroaromatic compounds for fluorescent probes and sensors due to its electron-withdrawing nitro group and aromatic structure. Also investigated for potential antitumor and antimicrobial activities in medicinal chemistry studies.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿400.00
inventory 100mg
10-20 days ฿402.00
inventory 250mg
10-20 days ฿1,130.00
inventory 1g
10-20 days ฿3,590.00
inventory 5g
10-20 days ฿16,090.00

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4-Methyl-5-nitro-1H-indole
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of indole-based drug candidates targeting inflammatory and neurological disorders. Serves as a building block in agrochemicals for creating novel pesticides with improved efficacy. Employed in research settings to explore nitroaromatic compounds for fluorescent probes and sensors due to its electron-withdrawing nitro group and aromatic structure. Also investigated for potential antitumor and antimicrobial activities in me
Used in the synthesis of pharmaceutical intermediates, particularly in the development of indole-based drug candidates targeting inflammatory and neurological disorders. Serves as a building block in agrochemicals for creating novel pesticides with improved efficacy. Employed in research settings to explore nitroaromatic compounds for fluorescent probes and sensors due to its electron-withdrawing nitro group and aromatic structure. Also investigated for potential antitumor and antimicrobial activities in medicinal chemistry studies.
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