4,5-Dibromothiophene-2-carbaldehyde

99%

Reagent Code: #177163
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CAS Number 38071-22-6

science Other reagents with same CAS 38071-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.94 g/mol
Formula C₅H₂Br₂OS
badge Registry Numbers
MDL Number MFCD00225242
thermostat Physical Properties
Melting Point 79-83 °C
Boiling Point 306.1±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.195±0.06 g/cm3(Predicted)
Storage 2-8°C, storage away from light, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of thiophene-based materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its functional groups allow for selective cross-coupling reactions, enabling the construction of complex π-conjugated systems. Also employed in the preparation of fluorescent dyes and sensors due to its ability to modify electronic properties in aromatic frameworks. Common in research settings for fabricating novel heterocyclic compounds with potential applications in optoelectronics and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿670.00
inventory 1g
10-20 days ฿1,180.00
inventory 5g
10-20 days ฿3,310.00
inventory 25g
10-20 days ฿15,370.00

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4,5-Dibromothiophene-2-carbaldehyde
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Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of thiophene-based materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its functional groups allow for selective cross-coupling reactions, enabling the construction of complex π-conjugated systems. Also employed in the preparation of fluorescent dyes and sensors due to its ability to modify electronic properties in aromatic frameworks. Common

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of thiophene-based materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its functional groups allow for selective cross-coupling reactions, enabling the construction of complex π-conjugated systems. Also employed in the preparation of fluorescent dyes and sensors due to its ability to modify electronic properties in aromatic frameworks. Common in research settings for fabricating novel heterocyclic compounds with potential applications in optoelectronics and medicinal chemistry.

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