Methyl 4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylate

≥98%

Reagent Code: #208119
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CAS Number 7767-60-4

science Other reagents with same CAS 7767-60-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.27 g/mol
Formula C₈H₈O₂S₂
thermostat Physical Properties
Melting Point 95-99°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic electronics as a building block for conjugated polymers, particularly in the development of conductive materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its fused heterocyclic structure enhances charge carrier mobility and stability when incorporated into polymer backbones. Also serves as an intermediate in synthesizing functionalized thiophene-based monomers for electroactive polymers. Shows potential in sensor applications due to its redox-active properties and ability to undergo controlled doping.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,240.00
inventory 1g
10-20 days ฿2,840.00
inventory 5g
10-20 days ฿11,610.00
inventory 10g
10-20 days ฿20,170.00
inventory 25g
10-20 days ฿48,560.00
Methyl 4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylate
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Used in organic electronics as a building block for conjugated polymers, particularly in the development of conductive materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its fused heterocyclic structure enhances charge carrier mobility and stability when incorporated into polymer backbones. Also serves as an intermediate in synthesizing functionalized thiophene-based monomers for electroactive polymers. Shows potential in sensor applications due to its redox-active p

Used in organic electronics as a building block for conjugated polymers, particularly in the development of conductive materials for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its fused heterocyclic structure enhances charge carrier mobility and stability when incorporated into polymer backbones. Also serves as an intermediate in synthesizing functionalized thiophene-based monomers for electroactive polymers. Shows potential in sensor applications due to its redox-active properties and ability to undergo controlled doping.

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