4-(THIOPHEN-3-YL)PHENOL

97%

Reagent Code: #242339
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CAS Number 29886-67-7

science Other reagents with same CAS 29886-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.23 g/mol
Formula C₁₀H₈OS
badge Registry Numbers
MDL Number MFCD06798133
thermostat Physical Properties
Melting Point 194-198 °C (lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in organic semiconductor materials due to the presence of the thiophene ring, which enhances electron delocalization and charge transport properties. Commonly employed as a building block in the synthesis of conjugated polymers for organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and organic light-emitting diodes (OLEDs). Also utilized in the development of sensors and electroactive materials owing to its redox activity and structural stability. Its phenolic group allows for easy functionalization, enabling incorporation into more complex molecular architectures for advanced electronic applications.

Additionally, used in pharmaceutical development owing to the phenolic and thiophene groups that enable interactions with biological targets, offering potential as antioxidants or anti-inflammatory agents. Also employed in laboratory research for modifying molecular structures to study structure-activity relationships (SAR).

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,210.00
inventory 5g
10-20 days ฿39,550.00

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4-(THIOPHEN-3-YL)PHENOL
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Used in organic semiconductor materials due to the presence of the thiophene ring, which enhances electron delocalization and charge transport properties. Commonly employed as a building block in the synthesis of conjugated polymers for organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and organic light-emitting diodes (OLEDs). Also utilized in the development of sensors and electroactive materials owing to its redox activity and structural stability. Its phenolic group allows for e

Used in organic semiconductor materials due to the presence of the thiophene ring, which enhances electron delocalization and charge transport properties. Commonly employed as a building block in the synthesis of conjugated polymers for organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and organic light-emitting diodes (OLEDs). Also utilized in the development of sensors and electroactive materials owing to its redox activity and structural stability. Its phenolic group allows for easy functionalization, enabling incorporation into more complex molecular architectures for advanced electronic applications.

Additionally, used in pharmaceutical development owing to the phenolic and thiophene groups that enable interactions with biological targets, offering potential as antioxidants or anti-inflammatory agents. Also employed in laboratory research for modifying molecular structures to study structure-activity relationships (SAR).

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