5-(Phenylethynyl)thiophene-2-carbaldehyde

98%

Reagent Code: #226963
fingerprint
CAS Number 17257-10-2

science Other reagents with same CAS 17257-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.27 g/mol
Formula C₁₃H₈OS
badge Registry Numbers
MDL Number MFCD00126374
thermostat Physical Properties
Boiling Point 388.6 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, storage away from light, inert atmosphere

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its aldehyde group enables further functionalization via condensation or nucleophilic addition, while the phenylethynyl-thiophene backbone supports extended π-conjugation, making it valuable in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Also employed in Suzuki and Stille coupling reactions to build complex aromatic systems for optoelectronic materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,850.00
inventory 1g
10-20 days ฿3,280.00
inventory 5g
10-20 days ฿16,020.00
5-(Phenylethynyl)thiophene-2-carbaldehyde
No image available

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its aldehyde group enables further functionalization via condensation or nucleophilic addition, while the phenylethynyl-thiophene backbone supports extended π-conjugation, making it valuable in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Also employed in Suzuki and Stille coupling reactions to buil

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated polymers and small molecule semiconductors for organic electronics. Its aldehyde group enables further functionalization via condensation or nucleophilic addition, while the phenylethynyl-thiophene backbone supports extended π-conjugation, making it valuable in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Also employed in Suzuki and Stille coupling reactions to build complex aromatic systems for optoelectronic materials.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...