13,6-N-SULFINYLACETAMIDOPENTACEN

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Reagent Code: #218583
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CAS Number 454675-76-4

science Other reagents with same CAS 454675-76-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.46 g/mol
Formula C₂₄H₁₇NO₂S
badge Registry Numbers
MDL Number MFCD08457646
thermostat Physical Properties
Melting Point 169-190 °C
Boiling Point 642.6±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.48±0.1 g/cm3(Predicted)
Storage -20°C

description Product Description

Used in organic semiconductor devices due to its extended pi-conjugated system, enabling efficient charge transport in thin-film transistors. Shows promise in flexible electronics and low-cost sensors owing to its thermal stability and ability to form uniform thin films. Also investigated for use in photovoltaic cells as a non-fullerene acceptor material, enhancing light absorption in the visible to near-infrared range. Its sulfinyl and acetamido functional groups improve solubility and film morphology, supporting solution-based fabrication techniques.

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inventory 100mg
10-20 days ฿49,880.00

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13,6-N-SULFINYLACETAMIDOPENTACEN
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Used in organic semiconductor devices due to its extended pi-conjugated system, enabling efficient charge transport in thin-film transistors. Shows promise in flexible electronics and low-cost sensors owing to its thermal stability and ability to form uniform thin films. Also investigated for use in photovoltaic cells as a non-fullerene acceptor material, enhancing light absorption in the visible to near-infrared range. Its sulfinyl and acetamido functional groups improve solubility and film morphology,

Used in organic semiconductor devices due to its extended pi-conjugated system, enabling efficient charge transport in thin-film transistors. Shows promise in flexible electronics and low-cost sensors owing to its thermal stability and ability to form uniform thin films. Also investigated for use in photovoltaic cells as a non-fullerene acceptor material, enhancing light absorption in the visible to near-infrared range. Its sulfinyl and acetamido functional groups improve solubility and film morphology, supporting solution-based fabrication techniques.

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