2-(5-Bromo-1H-indol-1-yl)ethanol

≥95%

Reagent Code: #148243
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CAS Number 148366-28-3

science Other reagents with same CAS 148366-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.10 g/mol
Formula C₁₀H₁₀BrNO
badge Registry Numbers
MDL Number MFCD20486677
thermostat Physical Properties
Boiling Point 383.3±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The bromoindole core makes it valuable in cross-coupling reactions, particularly in the development of serotonin receptor ligands and kinase inhibitors. The hydroxyl group allows for further functionalization, enabling attachment to other molecular frameworks. Commonly employed in medicinal chemistry for constructing indole-based drug candidates targeting neurological disorders and cancer. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,850.00
inventory 1g
10-20 days ฿7,700.00

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2-(5-Bromo-1H-indol-1-yl)ethanol
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The bromoindole core makes it valuable in cross-coupling reactions, particularly in the development of serotonin receptor ligands and kinase inhibitors. The hydroxyl group allows for further functionalization, enabling attachment to other molecular frameworks. Commonly employed in medicinal chemistry for constructing indole-based drug candidates targeting neurological disorders and cancer. Also utilized in the prepa

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The bromoindole core makes it valuable in cross-coupling reactions, particularly in the development of serotonin receptor ligands and kinase inhibitors. The hydroxyl group allows for further functionalization, enabling attachment to other molecular frameworks. Commonly employed in medicinal chemistry for constructing indole-based drug candidates targeting neurological disorders and cancer. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.

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