3,6-Dibromo-phenanthrenequinone

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Reagent Code: #170538
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CAS Number 53348-05-3

science Other reagents with same CAS 53348-05-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 366.007 g/mol
Formula C₁₄H₆Br₂O₂
badge Registry Numbers
MDL Number MFCD00451676
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a redox-active compound in organic semiconductors and electrochemical sensors due to its stable quinone structure and electron-accepting properties. It serves as a key intermediate in synthesizing functional dyes and photoresponsive materials. Its bromine substituents allow for further cross-coupling reactions, making it valuable in constructing complex conjugated systems for optoelectronic devices. Also explored in photoredox catalysis for organic transformations under light irradiation.

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Test Parameter Specification
Purity 97-100
Appearance Light orange to yellow crystal

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿1,670.00
inventory 25g
10-20 days ฿7,640.00

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3,6-Dibromo-phenanthrenequinone
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Used as a redox-active compound in organic semiconductors and electrochemical sensors due to its stable quinone structure and electron-accepting properties. It serves as a key intermediate in synthesizing functional dyes and photoresponsive materials. Its bromine substituents allow for further cross-coupling reactions, making it valuable in constructing complex conjugated systems for optoelectronic devices. Also explored in photoredox catalysis for organic transformations under light irradiation.

Used as a redox-active compound in organic semiconductors and electrochemical sensors due to its stable quinone structure and electron-accepting properties. It serves as a key intermediate in synthesizing functional dyes and photoresponsive materials. Its bromine substituents allow for further cross-coupling reactions, making it valuable in constructing complex conjugated systems for optoelectronic devices. Also explored in photoredox catalysis for organic transformations under light irradiation.

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