1,2-Di(thiophen-3-yl)ethane-1,2-dione

95%

Reagent Code: #177149
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CAS Number 7333-08-6

science Other reagents with same CAS 7333-08-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.28 g/mol
Formula C₁₀H₆O₂S₂
badge Registry Numbers
MDL Number MFCD19105338
thermostat Physical Properties
Melting Point 80 °C
Boiling Point 368.5±17.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.395±0.06 g/cm3(Predicted)
Storage Store at room temperature, away from light, dry seal

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated polymers and organic semiconductors. Its diketone functionality allows for condensation reactions to form heterocyclic structures, which are valuable in developing optoelectronic materials. Commonly employed in the synthesis of thiophene-based dyes and fluorescent probes due to its ability to extend π-conjugation. Also finds use in the fabrication of organic solar cells and thin-film transistors, where its electron-accepting properties enhance charge transport characteristics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,810.00
inventory 1g
10-20 days ฿7,570.00
inventory 5g
10-20 days ฿28,700.00

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1,2-Di(thiophen-3-yl)ethane-1,2-dione
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Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated polymers and organic semiconductors. Its diketone functionality allows for condensation reactions to form heterocyclic structures, which are valuable in developing optoelectronic materials. Commonly employed in the synthesis of thiophene-based dyes and fluorescent probes due to its ability to extend π-conjugation. Also finds use in the fabrication of organic solar cells and thin-film transistors, where its elec

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated polymers and organic semiconductors. Its diketone functionality allows for condensation reactions to form heterocyclic structures, which are valuable in developing optoelectronic materials. Commonly employed in the synthesis of thiophene-based dyes and fluorescent probes due to its ability to extend π-conjugation. Also finds use in the fabrication of organic solar cells and thin-film transistors, where its electron-accepting properties enhance charge transport characteristics.

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