thiophene-2,3-dicarbonitrile

97%

Reagent Code: #240961
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CAS Number 18853-42-4

science Other reagents with same CAS 18853-42-4

blur_circular Chemical Specifications

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Weight 134.158 g/mol
Formula C₆H₂N₂S
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of heterocyclic compounds with biological activity. Its electron-deficient aromatic structure makes it valuable in organic electronics, including the development of organic semiconductors and conductive materials. Also employed in the preparation of dyes and functional polymers due to its ability to participate in cyclization and condensation reactions. Its nitrile groups allow for further chemical modifications, enabling the creation of complex molecular architectures in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿33,480.00
thiophene-2,3-dicarbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of heterocyclic compounds with biological activity. Its electron-deficient aromatic structure makes it valuable in organic electronics, including the development of organic semiconductors and conductive materials. Also employed in the preparation of dyes and functional polymers due to its ability to participate in cyclization and condensation reactions. Its nitrile groups allow for further che

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of heterocyclic compounds with biological activity. Its electron-deficient aromatic structure makes it valuable in organic electronics, including the development of organic semiconductors and conductive materials. Also employed in the preparation of dyes and functional polymers due to its ability to participate in cyclization and condensation reactions. Its nitrile groups allow for further chemical modifications, enabling the creation of complex molecular architectures in medicinal chemistry research.

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