3,7-Dibromodibenzothiophene 5,5-Dioxide

97%

Reagent Code: #174527
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CAS Number 83834-12-2

science Other reagents with same CAS 83834-12-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 374.05 g/mol
Formula C₁₂H₆Br₂O₂S
badge Registry Numbers
MDL Number MFCD00227704
thermostat Physical Properties
Melting Point 312°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and functional materials. Its brominated structure allows for cross-coupling reactions, making it valuable in constructing complex aromatic systems. Commonly employed in the preparation of conjugated polymers and small-molecule semiconductors for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The sulfone group enhances electron-accepting properties, contributing to improved charge transport characteristics in electronic materials.

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inventory 200mg
10-20 days ฿6,490.00

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3,7-Dibromodibenzothiophene 5,5-Dioxide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and functional materials. Its brominated structure allows for cross-coupling reactions, making it valuable in constructing complex aromatic systems. Commonly employed in the preparation of conjugated polymers and small-molecule semiconductors for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The sulfone group enhances electron-accepting properties, cont

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and functional materials. Its brominated structure allows for cross-coupling reactions, making it valuable in constructing complex aromatic systems. Commonly employed in the preparation of conjugated polymers and small-molecule semiconductors for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The sulfone group enhances electron-accepting properties, contributing to improved charge transport characteristics in electronic materials.

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