4,7-Bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-5,6-difluorobenzo[c][1,2,5]thiadiazole

98%

Reagent Code: #146931
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CAS Number 1293389-32-8

science Other reagents with same CAS 1293389-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 718.62 g/mol
Formula C₃₀H₃₆Br₂F₂N₂S₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in organic electronics, this compound serves as a key building block in high-performance organic semiconductors. It is especially effective in the development of organic photovoltaic (OPV) cells, where it acts as an electron-accepting material in active layers, enhancing light absorption and charge transport. Its strong electron-deficient character and broad absorption spectrum improve power conversion efficiency in solar cells. Additionally, it is employed in organic field-effect transistors (OFETs) and as a component in low-bandgap polymers for near-infrared applications. The presence of bromine allows for further functionalization via cross-coupling reactions, enabling tailored modifications for specific electronic properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,898.50
inventory 250mg
10-20 days ฿8,734.00
inventory 1g
10-20 days ฿27,494.50

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4,7-Bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-5,6-difluorobenzo[c][1,2,5]thiadiazole
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Used primarily in organic electronics, this compound serves as a key building block in high-performance organic semiconductors. It is especially effective in the development of organic photovoltaic (OPV) cells, where it acts as an electron-accepting material in active layers, enhancing light absorption and charge transport. Its strong electron-deficient character and broad absorption spectrum improve power conversion efficiency in solar cells. Additionally, it is employed in organic field-effect transist

Used primarily in organic electronics, this compound serves as a key building block in high-performance organic semiconductors. It is especially effective in the development of organic photovoltaic (OPV) cells, where it acts as an electron-accepting material in active layers, enhancing light absorption and charge transport. Its strong electron-deficient character and broad absorption spectrum improve power conversion efficiency in solar cells. Additionally, it is employed in organic field-effect transistors (OFETs) and as a component in low-bandgap polymers for near-infrared applications. The presence of bromine allows for further functionalization via cross-coupling reactions, enabling tailored modifications for specific electronic properties.

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