5,5',5''-(Nitrilotris(benzene-4,1-diyl))tris(thiophene-2-carbaldehyde)

97%

Reagent Code: #218821
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CAS Number 883236-47-3

science Other reagents with same CAS 883236-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 575.72 g/mol
Formula C₃₃H₂₁NO₃S₃
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used in organic electronics as a key intermediate for synthesizing conjugated polymers and small-molecule semiconductors. Its aldehyde functional groups allow for easy extension of π-conjugated systems through cross-coupling or condensation reactions, making it valuable in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The presence of multiple thiophene units enhances charge carrier mobility, while the tri-branched structure supports three-dimensional conjugation, improving film morphology and device performance. Also employed in sensing applications due to its fluorescence properties when modified into fluorescent probes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿940.00
inventory 250mg
10-20 days ฿1,590.00
inventory 1g
10-20 days ฿5,510.00
inventory 5g
10-20 days ฿26,700.00
5,5',5''-(Nitrilotris(benzene-4,1-diyl))tris(thiophene-2-carbaldehyde)
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Used in organic electronics as a key intermediate for synthesizing conjugated polymers and small-molecule semiconductors. Its aldehyde functional groups allow for easy extension of π-conjugated systems through cross-coupling or condensation reactions, making it valuable in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The presence of multiple thiophene units enhances charge carrier mobility, while the tri-branched structure supports three-dimensional conjugati

Used in organic electronics as a key intermediate for synthesizing conjugated polymers and small-molecule semiconductors. Its aldehyde functional groups allow for easy extension of π-conjugated systems through cross-coupling or condensation reactions, making it valuable in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The presence of multiple thiophene units enhances charge carrier mobility, while the tri-branched structure supports three-dimensional conjugation, improving film morphology and device performance. Also employed in sensing applications due to its fluorescence properties when modified into fluorescent probes.

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