3-(2-Aminoethyl)-1H-indole-5-carbonitrile hydrochloride

≥95%

Reagent Code: #120065
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CAS Number 101831-71-4

science Other reagents with same CAS 101831-71-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.69 g/mol
Formula C₁₁H₁₂ClN₃
badge Registry Numbers
MDL Number MFCD01719136
thermostat Physical Properties
Boiling Point 423.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in biochemical research as a precursor or intermediate in the synthesis of more complex molecules, particularly those targeting neurological pathways. It is often employed in the development of compounds that interact with serotonin receptors, due to its structural similarity to serotonin. Researchers use it to study and design potential therapeutic agents for conditions such as depression, anxiety, and other mood disorders. Additionally, it serves as a valuable tool in organic synthesis for creating indole derivatives, which are significant in medicinal chemistry for their diverse biological activities. Its hydrochloride form enhances solubility, making it easier to handle in experimental settings.

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Test Parameter Specification
Appearance Yellow Powder
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,894.00
inventory 250mg
10-20 days ฿13,779.00

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3-(2-Aminoethyl)-1H-indole-5-carbonitrile hydrochloride
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This compound is primarily utilized in biochemical research as a precursor or intermediate in the synthesis of more complex molecules, particularly those targeting neurological pathways. It is often employed in the development of compounds that interact with serotonin receptors, due to its structural similarity to serotonin. Researchers use it to study and design potential therapeutic agents for conditions such as depression, anxiety, and other mood disorders. Additionally, it serves as a valuable tool in organic synthesis for creating indole derivatives, which are significant in medicinal chemistry for their diverse biological activities. Its hydrochloride form enhances solubility, making it easier to handle in experimental settings.
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