1-(4-(Benzo[d]oxazol-2-yl)phenyl)-1H-pyrrole-2,5-dione

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Reagent Code: #146748
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CAS Number 16707-41-8

science Other reagents with same CAS 16707-41-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.27 g/mol
Formula C₁₇H₁₀N₂O₃
thermostat Physical Properties
Melting Point 211-213°C
Boiling Point 462.7°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic electronics as a building block for conjugated polymers and small molecules in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its rigid aromatic structure and electron-deficient nature enhance charge transport properties and improve device efficiency. Commonly employed in donor-acceptor copolymers to tune bandgap and energy levels for better light absorption and electron mobility. Also explored in fluorescent probes and sensors due to its luminescent characteristics in solid and solution states.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,340.00
inventory 250mg
10-20 days ฿8,670.00

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1-(4-(Benzo[d]oxazol-2-yl)phenyl)-1H-pyrrole-2,5-dione
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Used in organic electronics as a building block for conjugated polymers and small molecules in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its rigid aromatic structure and electron-deficient nature enhance charge transport properties and improve device efficiency. Commonly employed in donor-acceptor copolymers to tune bandgap and energy levels for better light absorption and electron mobility. Also explored in fluorescent probes and sensors due to its luminescent characteristi

Used in organic electronics as a building block for conjugated polymers and small molecules in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its rigid aromatic structure and electron-deficient nature enhance charge transport properties and improve device efficiency. Commonly employed in donor-acceptor copolymers to tune bandgap and energy levels for better light absorption and electron mobility. Also explored in fluorescent probes and sensors due to its luminescent characteristics in solid and solution states.

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