6-Nitro-1H-indole-3-carbonitrile

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Reagent Code: #214830
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CAS Number 4769-99-7

science Other reagents with same CAS 4769-99-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.16 g/mol
Formula C₉H₅N₃O₂
badge Registry Numbers
MDL Number MFCD15527153
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based bioactive compounds. It serves as a building block in medicinal chemistry for creating inhibitors targeting enzymes and receptors involved in inflammatory and neurological pathways. Also applied in research for the preparation of fluorescent probes due to its electron-withdrawing nitrile and nitro groups, which enhance photophysical properties. Additionally, it has been explored in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,250.00
inventory 250mg
10-20 days ฿12,300.00
inventory 1g
10-20 days ฿33,200.00

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6-Nitro-1H-indole-3-carbonitrile
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based bioactive compounds. It serves as a building block in medicinal chemistry for creating inhibitors targeting enzymes and receptors involved in inflammatory and neurological pathways. Also applied in research for the preparation of fluorescent probes due to its electron-withdrawing nitrile and nitro groups, which enhance photophysical properties. Additionally, it has been explored in agrochemical re

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based bioactive compounds. It serves as a building block in medicinal chemistry for creating inhibitors targeting enzymes and receptors involved in inflammatory and neurological pathways. Also applied in research for the preparation of fluorescent probes due to its electron-withdrawing nitrile and nitro groups, which enhance photophysical properties. Additionally, it has been explored in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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