ethyl 3-methyl-5-[(3-methylthiophene-2-carbonyl)amino]thiophene-2-carboxylate

98%

Reagent Code: #245634
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CAS Number 378223-81-5

science Other reagents with same CAS 378223-81-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.4 g/mol
Formula C₁₄H₁₅NO₃S₂
thermostat Physical Properties
Boiling Point 381.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.321±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its structure supports efficient π-π stacking and charge transport, making it valuable in creating high-performance electronic materials. Commonly employed in cross-coupling reactions to build complex thiophene-based frameworks with tunable electronic properties. Also utilized in research settings for designing novel donor-acceptor copolymers aimed at improving solar cell efficiency and flexibility in electronic devices.

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inventory 5mg
10-20 days ฿29,690.00

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ethyl 3-methyl-5-[(3-methylthiophene-2-carbonyl)amino]thiophene-2-carboxylate
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Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its structure supports efficient π-π stacking and charge transport, making it valuable in creating high-performance electronic materials. Commonly employed in cross-coupling reactions to build complex thiophene-based frameworks with tunable electronic properties. Also utilized in research settings for d

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its structure supports efficient π-π stacking and charge transport, making it valuable in creating high-performance electronic materials. Commonly employed in cross-coupling reactions to build complex thiophene-based frameworks with tunable electronic properties. Also utilized in research settings for designing novel donor-acceptor copolymers aimed at improving solar cell efficiency and flexibility in electronic devices.

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