Thieno[2,3-b]thiophene-2-carboxylic acid

95%

Reagent Code: #242692
label
Alias thieno[2,3-B]thieno-2-carboxylic acid; thieno[2,3-B]thieno-2-carboxylic acid
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CAS Number 14756-75-3

science Other reagents with same CAS 14756-75-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.24 g/mol
Formula C₇H₄O₂S₂
badge Registry Numbers
MDL Number MFCD00111552
thermostat Physical Properties
Boiling Point 389.495°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-conjugation and promotes strong intermolecular stacking, improving charge carrier mobility. Also employed in the preparation of functional materials for sensors and optoelectronic devices due to its favorable electronic properties and chemical stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,760.00
inventory 250mg
10-20 days ฿8,710.00
inventory 1g
10-20 days ฿19,970.00

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Thieno[2,3-b]thiophene-2-carboxylic acid
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Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-conjugation and promotes strong intermolecular stacking, improving charge carrier mobility. Also employed in the preparation of functional materials for sensors and optoelectronic devices due to its favorable electronic properties and chemical stab

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-conjugation and promotes strong intermolecular stacking, improving charge carrier mobility. Also employed in the preparation of functional materials for sensors and optoelectronic devices due to its favorable electronic properties and chemical stability.

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