4-(Di(1H-indol-3-yl)methyl)phenol

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Reagent Code: #46449
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CAS Number 151358-47-3

science Other reagents with same CAS 151358-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.41 g/mol
Formula C₂₃H₁₈N₂O
badge Registry Numbers
MDL Number MFCD03723253
thermostat Physical Properties
Boiling Point 610.2±50.0℃at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in organic synthesis for the development of fluorescent probes due to its unique indole-based structure, which exhibits strong fluorescence properties. It is also explored in the design of bioactive molecules, particularly in pharmaceutical research, for its potential antioxidant, anti-inflammatory, and anticancer activities. Additionally, it serves as a building block in the creation of advanced materials for optoelectronic applications, leveraging its ability to form stable, conjugated systems.

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Test Parameter Specification
Appearance Light Pink Powder
Purity (%) 96.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,146.00
inventory 250mg
10-20 days ฿3,132.00

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4-(Di(1H-indol-3-yl)methyl)phenol
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Used in organic synthesis for the development of fluorescent probes due to its unique indole-based structure, which exhibits strong fluorescence properties. It is also explored in the design of bioactive molecules, particularly in pharmaceutical research, for its potential antioxidant, anti-inflammatory, and anticancer activities. Additionally, it serves as a building block in the creation of advanced materials for optoelectronic applications, leveraging its ability to form stable, conjugated systems.

Used in organic synthesis for the development of fluorescent probes due to its unique indole-based structure, which exhibits strong fluorescence properties. It is also explored in the design of bioactive molecules, particularly in pharmaceutical research, for its potential antioxidant, anti-inflammatory, and anticancer activities. Additionally, it serves as a building block in the creation of advanced materials for optoelectronic applications, leveraging its ability to form stable, conjugated systems.

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