6-Chloro-1H-indole-3-carbonitrile

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Reagent Code: #81516
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CAS Number 194490-17-0

science Other reagents with same CAS 194490-17-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.6 g/mol
Formula C₉H₅ClN₂
thermostat Physical Properties
Boiling Point 383.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active molecules, particularly those targeting neurological and oncological disorders. Its indole core structure makes it valuable for developing compounds with potential therapeutic properties, such as serotonin receptor modulators or kinase inhibitors. Researchers also utilize it in the synthesis of agrochemicals, where its chemical framework contributes to the creation of pesticides or herbicides. Additionally, its reactivity allows for further functionalization, enabling the development of novel chemical entities for drug discovery and material science applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,905.00
inventory 250mg
10-20 days ฿7,353.00
inventory 1g
10-20 days ฿18,369.00

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6-Chloro-1H-indole-3-carbonitrile
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This compound is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active molecules, particularly those targeting neurological and oncological disorders. Its indole core structure makes it valuable for developing compounds with potential therapeutic properties, such as serotonin receptor modulators or kinase inhibitors. Researchers also utilize it in the synthesis of agrochemicals, where its chemical framework contri

This compound is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active molecules, particularly those targeting neurological and oncological disorders. Its indole core structure makes it valuable for developing compounds with potential therapeutic properties, such as serotonin receptor modulators or kinase inhibitors. Researchers also utilize it in the synthesis of agrochemicals, where its chemical framework contributes to the creation of pesticides or herbicides. Additionally, its reactivity allows for further functionalization, enabling the development of novel chemical entities for drug discovery and material science applications.

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