2-(4-Bromophenyl)thiophene

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Reagent Code: #145326
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CAS Number 40133-22-0

science Other reagents with same CAS 40133-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.13 g/mol
Formula C₁₀H₇BrS
thermostat Physical Properties
Melting Point 95-99°C
Boiling Point 307°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic semiconductor materials due to its conjugated structure, enabling applications in organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Serves as a building block in the synthesis of conjugated polymers and small molecules for optoelectronic devices. Common intermediate in cross-coupling reactions, such as Suzuki or Stille couplings, to form extended π-conjugated systems for use in photovoltaic cells and sensors. Its bromine functionality allows for easy functionalization and incorporation into larger aromatic frameworks.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿550.00
inventory 1g
10-20 days ฿1,630.00

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2-(4-Bromophenyl)thiophene
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Used in organic semiconductor materials due to its conjugated structure, enabling applications in organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Serves as a building block in the synthesis of conjugated polymers and small molecules for optoelectronic devices. Common intermediate in cross-coupling reactions, such as Suzuki or Stille couplings, to form extended π-conjugated systems for use in photovoltaic cells and sensors. Its bromine functionality allows for easy func

Used in organic semiconductor materials due to its conjugated structure, enabling applications in organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Serves as a building block in the synthesis of conjugated polymers and small molecules for optoelectronic devices. Common intermediate in cross-coupling reactions, such as Suzuki or Stille couplings, to form extended π-conjugated systems for use in photovoltaic cells and sensors. Its bromine functionality allows for easy functionalization and incorporation into larger aromatic frameworks.

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