(E)-3-(4-methoxyphenyl)-2-(pyridin-2-yl)acrylonitrile

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Reagent Code: #180804
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CAS Number 22346-01-6

science Other reagents with same CAS 22346-01-6

blur_circular Chemical Specifications

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Weight 236.273 g/mol
Formula C₁₅H₁₂N₂O
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic electronics as a key intermediate in the synthesis of conjugated polymers and small molecule semiconductors. Its extended π-conjugated system enhances charge transport properties, making it suitable for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Also employed in the development of fluorescent sensors due to its strong emission characteristics upon structural modification. Shows potential in medicinal chemistry as a scaffold for kinase inhibitors, particularly in anticancer research where the nitrile and vinyl groups interact with biological targets through hydrogen bonding and dipole interactions.

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inventory 1g
10-20 days ฿22,500.00

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(E)-3-(4-methoxyphenyl)-2-(pyridin-2-yl)acrylonitrile
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Used in organic electronics as a key intermediate in the synthesis of conjugated polymers and small molecule semiconductors. Its extended π-conjugated system enhances charge transport properties, making it suitable for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Also employed in the development of fluorescent sensors due to its strong emission characteristics upon structural modification. Shows potential in medicinal chemistry as a scaffold for kinase inhibi

Used in organic electronics as a key intermediate in the synthesis of conjugated polymers and small molecule semiconductors. Its extended π-conjugated system enhances charge transport properties, making it suitable for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Also employed in the development of fluorescent sensors due to its strong emission characteristics upon structural modification. Shows potential in medicinal chemistry as a scaffold for kinase inhibitors, particularly in anticancer research where the nitrile and vinyl groups interact with biological targets through hydrogen bonding and dipole interactions.

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