5-Bromo-1-ethyl-1H-indole

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Reagent Code: #48837
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CAS Number 195253-49-7

science Other reagents with same CAS 195253-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.10 g/mol
Formula C₁₀H₁₀BrN
badge Registry Numbers
MDL Number MFCD04344211
thermostat Physical Properties
Boiling Point 311.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

Used in organic synthesis as a building block for creating more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity, such as inhibitors or receptor modulators. Its indole structure makes it valuable in the study of serotonin-related pathways, contributing to research on neurological disorders. Additionally, it is employed in the synthesis of fluorescent dyes and other materials for analytical and industrial applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿14,697.00
inventory 10g
10-20 days ฿20,997.00
inventory 1g
10-20 days ฿7,344.00

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5-Bromo-1-ethyl-1H-indole
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Used in organic synthesis as a building block for creating more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity, such as inhibitors or receptor modulators. Its indole structure makes it valuable in the study of serotonin-related pathways, contributing to research on neurological disorders. Additionally, it is employed in the synthesis of fluorescent dyes and other mat

Used in organic synthesis as a building block for creating more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity, such as inhibitors or receptor modulators. Its indole structure makes it valuable in the study of serotonin-related pathways, contributing to research on neurological disorders. Additionally, it is employed in the synthesis of fluorescent dyes and other materials for analytical and industrial applications.

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