4-Phenylthiophene-2-carbaldehyde

97%

Reagent Code: #226648
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CAS Number 26170-87-6

science Other reagents with same CAS 26170-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.25 g/mol
Formula C₁₁H₈OS
badge Registry Numbers
MDL Number MFCD03701610
thermostat Physical Properties
Melting Point 67 - 71 ℃ - lit.
Boiling Point 312.4 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.207 g/cm3
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of polythiophene derivatives for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its aldehyde functionality allows for further chemical modification, enabling the introduction of various side chains or functional groups to tune electronic properties. Also employed in the preparation of fluorescent dyes and sensors due to its aromatic and electron-rich structure. Plays a role in cross-coupling reactions for constructing complex π-conjugated systems used in electronic devices.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,540.00
1g
10-20 days ฿2,940.00
5g
10-20 days ฿11,930.00
4-Phenylthiophene-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 polythiophene derivatives for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its aldehyde functionality allows for further chemical modification, enabling the introduction of various side chains or functional groups to tune electronic properties. Also employed in the preparation of fluorescent dyes and sensors due to its aromatic and electron-rich stru

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of polythiophene derivatives for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its aldehyde functionality allows for further chemical modification, enabling the introduction of various side chains or functional groups to tune electronic properties. Also employed in the preparation of fluorescent dyes and sensors due to its aromatic and electron-rich structure. Plays a role in cross-coupling reactions for constructing complex π-conjugated systems used in electronic devices.

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