Methyl thieno[3,4-b]thiophene-2-carboxylate

≥95%

Reagent Code: #208825
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CAS Number 14630-09-2

science Other reagents with same CAS 14630-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.26 g/mol
Formula C₈H₆O₂S₂
badge Registry Numbers
MDL Number MFCD28015646
thermostat Physical Properties
Boiling Point 315.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed from light

description Product Description

Used in organic electronics as a building block for conjugated polymers, particularly in the development of donor-acceptor copolymers for organic solar cells. Its fused heterocyclic structure enhances π-conjugation and promotes charge carrier mobility when incorporated into polymer backbones. It is also employed in the synthesis of functional monomers for electropolymerization, leading to conductive films with potential use in sensors and optoelectronic devices. The ester group allows for further chemical modification, enabling tuning of solubility and electronic properties in advanced materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,460.00
250mg
10-20 days ฿12,680.00
1g
10-20 days ฿31,690.00
Methyl thieno[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 donor-acceptor copolymers for organic solar cells. Its fused heterocyclic structure enhances π-conjugation and promotes charge carrier mobility when incorporated into polymer backbones. It is also employed in the synthesis of functional monomers for electropolymerization, leading to conductive films with potential use in sensors and optoelectronic devices. The ester group allows for further chemica

Used in organic electronics as a building block for conjugated polymers, particularly in the development of donor-acceptor copolymers for organic solar cells. Its fused heterocyclic structure enhances π-conjugation and promotes charge carrier mobility when incorporated into polymer backbones. It is also employed in the synthesis of functional monomers for electropolymerization, leading to conductive films with potential use in sensors and optoelectronic devices. The ester group allows for further chemical modification, enabling tuning of solubility and electronic properties in advanced materials.

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