4-Nitrothiophene-2-carbonitrile

95%

Reagent Code: #218826
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CAS Number 42137-24-6

science Other reagents with same CAS 42137-24-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.15 g/mol
Formula C₅H₂N₂O₂S
badge Registry Numbers
MDL Number MFCD03426907
thermostat Physical Properties
Boiling Point 276.1 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antifungal properties. Its structure allows for further functionalization, making it valuable in creating heterocyclic compounds for drug discovery. Also employed in materials science for the preparation of organic semiconductors and conductive polymers due to the electron-withdrawing nature of the nitro and nitrile groups combined with the thiophene ring. Commonly utilized in cross-coupling reactions to build complex aromatic systems in research laboratories.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿670.00
inventory 250mg
10-20 days ฿1,620.00
inventory 1g
10-20 days ฿5,570.00
4-Nitrothiophene-2-carbonitrile
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antifungal properties. Its structure allows for further functionalization, making it valuable in creating heterocyclic compounds for drug discovery. Also employed in materials science for the preparation of organic semiconductors and conductive polymers due to the electron-withdrawing nature of the nitro and nitrile groups combined with the thiophene

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antifungal properties. Its structure allows for further functionalization, making it valuable in creating heterocyclic compounds for drug discovery. Also employed in materials science for the preparation of organic semiconductors and conductive polymers due to the electron-withdrawing nature of the nitro and nitrile groups combined with the thiophene ring. Commonly utilized in cross-coupling reactions to build complex aromatic systems in research laboratories.

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