4-Phenylthiophene-2-carboxylic acid

96%

Reagent Code: #226689
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CAS Number 21676-88-0

science Other reagents with same CAS 21676-88-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.25 g/mol
Formula C₁₁H₈O₂S
badge Registry Numbers
MDL Number MFCD03408007
thermostat Physical Properties
Melting Point 164 - 170 ℃
Boiling Point 364.2 ℃ at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure supports extended π-conjugation, enhancing charge transport properties in semiconductor materials. Also employed in the preparation of functionalized thiophene-based copolymers due to its ability to undergo palladium-catalyzed coupling reactions. Additionally, it serves as a building block in pharmaceutical research for developing bioactive molecules with potential anti-inflammatory or antimicrobial activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿820.00
250mg
10-20 days ฿1,290.00
1g
10-20 days ฿4,930.00
4-Phenylthiophene-2-carboxylic acid
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Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure supports extended π-conjugation, enhancing charge transport properties in semiconductor materials. Also employed in the preparation of functionalized thiophene-based copolymers due to its ability to undergo palladium-catalyzed coupling reactions. Additionally, it serves as a building block in pharmaceutical resear

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure supports extended π-conjugation, enhancing charge transport properties in semiconductor materials. Also employed in the preparation of functionalized thiophene-based copolymers due to its ability to undergo palladium-catalyzed coupling reactions. Additionally, it serves as a building block in pharmaceutical research for developing bioactive molecules with potential anti-inflammatory or antimicrobial activity.

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