4-[Bis(2-methyl-1H-indol-3-yl)methyl]-2-methoxyphenol

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Reagent Code: #149132
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CAS Number 342594-80-3

science Other reagents with same CAS 342594-80-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 396.4810 g/mol
Formula C₂₆H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD07784402
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in research settings as a fluorescent probe due to its strong emission properties when excited. Its structure allows for interaction with biomolecules, making it useful in studying protein binding and conformational changes. Also investigated for its potential as a sensor in detecting metal ions in environmental and biological samples. Shows promise in photodynamic therapy research because of its ability to generate reactive oxygen species under light exposure. Additionally, its indole-based framework supports exploration in developing novel anti-inflammatory and anticancer agents.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿45,090.00
inventory 50mg
10-20 days ฿51,200.00
inventory 100mg
10-20 days ฿80,000.00

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4-[Bis(2-methyl-1H-indol-3-yl)methyl]-2-methoxyphenol
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Used primarily in research settings as a fluorescent probe due to its strong emission properties when excited. Its structure allows for interaction with biomolecules, making it useful in studying protein binding and conformational changes. Also investigated for its potential as a sensor in detecting metal ions in environmental and biological samples. Shows promise in photodynamic therapy research because of its ability to generate reactive oxygen species under light exposure. Additionally, its indole-bas

Used primarily in research settings as a fluorescent probe due to its strong emission properties when excited. Its structure allows for interaction with biomolecules, making it useful in studying protein binding and conformational changes. Also investigated for its potential as a sensor in detecting metal ions in environmental and biological samples. Shows promise in photodynamic therapy research because of its ability to generate reactive oxygen species under light exposure. Additionally, its indole-based framework supports exploration in developing novel anti-inflammatory and anticancer agents.

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