4-Iodothiophene-2-carbaldehyde

95%

Reagent Code: #199731
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CAS Number 18812-38-9

science Other reagents with same CAS 18812-38-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.05 g/mol
Formula C₅H₃IOS
badge Registry Numbers
MDL Number MFCD13659397
thermostat Physical Properties
Boiling Point 298.0±25.0°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the fabrication of thiophene-based materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its iodo functional group allows for efficient cross-coupling reactions, such as Suzuki or Stille couplings, enabling the construction of complex π-conjugated systems. Also employed in the development of fluorescent dyes and sensors due to the thiophene ring’s electronic properties. Its aldehyde group provides a site for further functionalization, making it valuable in medicinal chemistry for building bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,400.00
4-Iodothiophene-2-carbaldehyde
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Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the fabrication of thiophene-based materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its iodo functional group allows for efficient cross-coupling reactions, such as Suzuki or Stille couplings, enabling the construction of complex π-conjugated systems. Also employed in the development of fluorescent dyes and sensors due to the thiophene ring’s electronic pr

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the fabrication of thiophene-based materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its iodo functional group allows for efficient cross-coupling reactions, such as Suzuki or Stille couplings, enabling the construction of complex π-conjugated systems. Also employed in the development of fluorescent dyes and sensors due to the thiophene ring’s electronic properties. Its aldehyde group provides a site for further functionalization, making it valuable in medicinal chemistry for building bioactive molecules.

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