thiophene-2,5-dicarbonyl dichloride

98%

Reagent Code: #242427
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CAS Number 3857-36-1

science Other reagents with same CAS 3857-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.04 g/mol
Formula C₆H₂O₂SCl₂
thermostat Physical Properties
Melting Point 43-47 °C(lit.)
Boiling Point 150-152 °C at 11 mmHg (lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in the production of polythiophene derivatives. These polymers are essential in organic solar cells, thin-film transistors, and light-emitting diodes due to their excellent charge transport properties and tunable band gaps. The compound’s reactive acid chloride groups allow for efficient coupling with various comonomers, enabling precise control over polymer structure and functionality. It is also employed in the preparation of functional organic materials for sensors and electrochromic devices.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,380.00

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thiophene-2,5-dicarbonyl dichloride
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Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in the production of polythiophene derivatives. These polymers are essential in organic solar cells, thin-film transistors, and light-emitting diodes due to their excellent charge transport properties and tunable band gaps. The compound’s reactive acid chloride groups allow for efficient coupling with various comonomers, enabling precise control over polymer structure and functionality. It is also emp

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in the production of polythiophene derivatives. These polymers are essential in organic solar cells, thin-film transistors, and light-emitting diodes due to their excellent charge transport properties and tunable band gaps. The compound’s reactive acid chloride groups allow for efficient coupling with various comonomers, enabling precise control over polymer structure and functionality. It is also employed in the preparation of functional organic materials for sensors and electrochromic devices.

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