5-Nitrothiophene-2-carbonitrile

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Reagent Code: #216961
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CAS Number 16689-02-4

science Other reagents with same CAS 16689-02-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.1500 g/mol
Formula C₅H₂N₂O₂S
badge Registry Numbers
MDL Number MFCD00052401
thermostat Physical Properties
Melting Point 42-46 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in creating biologically active molecules. Commonly employed in heterocyclic chemistry to build complex thiophene-based compounds with potential use in medicinal and agrochemical research. Also utilized in the preparation of organic semiconductors due to the electron-withdrawing nature of the nitro and nitrile groups, enhancing electronic properties in materials science applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,670.00
inventory 25g
10-20 days ฿12,020.00

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5-Nitrothiophene-2-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in creating biologically active molecules. Commonly employed in heterocyclic chemistry to build complex thiophene-based compounds with potential use in medicinal and agrochemical research. Also utilized in the preparation of organic semiconductors due to the electron-withdrawing nature of the nitro and nitr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in creating biologically active molecules. Commonly employed in heterocyclic chemistry to build complex thiophene-based compounds with potential use in medicinal and agrochemical research. Also utilized in the preparation of organic semiconductors due to the electron-withdrawing nature of the nitro and nitrile groups, enhancing electronic properties in materials science applications.

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