2,6-Dibromonaphthalene-1,4,5,8-tetracarboxylic Dianhydride

95%

Reagent Code: #173940
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CAS Number 83204-68-6

science Other reagents with same CAS 83204-68-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 425.99 g/mol
Formula C₁₄H₂Br₂O₆
badge Registry Numbers
MDL Number MFCD00406909
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in the synthesis of high-performance organic semiconductors and n-type conjugated polymers for electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-π stacking, improving charge carrier mobility. Also serves as a building block in the preparation of perylene diimide (PDI) derivatives, which are valued for their thermal stability, strong electron-accepting properties, and use in dyes, pigments, and fluorescent probes. Additionally, employed in coordination chemistry to form metal-organic frameworks (MOFs) with unique optoelectronic behaviors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,800.00
inventory 1g
10-20 days ฿5,300.00
inventory 5g
10-20 days ฿19,700.00
inventory 25g
10-20 days ฿66,160.00

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2,6-Dibromonaphthalene-1,4,5,8-tetracarboxylic Dianhydride
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Used primarily in the synthesis of high-performance organic semiconductors and n-type conjugated polymers for electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-π stacking, improving charge carrier mobility. Also serves as a building block in the preparation of perylene diimide (PDI) derivatives, which are valued for their thermal stability, strong electron-accepting properties, and use in dyes, pigments, and fluore

Used primarily in the synthesis of high-performance organic semiconductors and n-type conjugated polymers for electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-π stacking, improving charge carrier mobility. Also serves as a building block in the preparation of perylene diimide (PDI) derivatives, which are valued for their thermal stability, strong electron-accepting properties, and use in dyes, pigments, and fluorescent probes. Additionally, employed in coordination chemistry to form metal-organic frameworks (MOFs) with unique optoelectronic behaviors.

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