Methyl 2-(furan-2-carboxamido)-4-phenylthiophene-3-carboxylate

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Reagent Code: #129734
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CAS Number 315679-74-4

science Other reagents with same CAS 315679-74-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.35 g/mol
Formula C₁₇H₁₃NO₄S
thermostat Physical Properties
Boiling Point 406.5±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.342±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in organic semiconductor materials due to its extended π-conjugated system, enhancing electron transport in thin-film transistors. Employed as a key intermediate in synthesizing bioactive heterocyclic compounds, particularly in developing anti-inflammatory and antimicrobial agents. Its furan and thiophene rings contribute to photoluminescent properties, making it suitable for OLEDs and fluorescent sensors. Also applied in dye-sensitized solar cells as a sensitizer component for improved light absorption and charge transfer efficiency.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,490.00
inventory 100mg
10-20 days ฿18,190.00

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Methyl 2-(furan-2-carboxamido)-4-phenylthiophene-3-carboxylate
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Used in organic semiconductor materials due to its extended π-conjugated system, enhancing electron transport in thin-film transistors. Employed as a key intermediate in synthesizing bioactive heterocyclic compounds, particularly in developing anti-inflammatory and antimicrobial agents. Its furan and thiophene rings contribute to photoluminescent properties, making it suitable for OLEDs and fluorescent sensors. Also applied in dye-sensitized solar cells as a sensitizer component for improved light absorp

Used in organic semiconductor materials due to its extended π-conjugated system, enhancing electron transport in thin-film transistors. Employed as a key intermediate in synthesizing bioactive heterocyclic compounds, particularly in developing anti-inflammatory and antimicrobial agents. Its furan and thiophene rings contribute to photoluminescent properties, making it suitable for OLEDs and fluorescent sensors. Also applied in dye-sensitized solar cells as a sensitizer component for improved light absorption and charge transfer efficiency.

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