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CAS 17989-89-8

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2,5-Diamino-3,4-thiophenedicarbonitrile

Description:
2,5-Diamino-3,4-thiophenedicarbonitrile is an organic compound characterized by its unique structure, which includes a thiophene ring and two amino groups along with two cyano groups. This compound is typically a solid at room temperature and may exhibit a range of colors depending on its purity and form. It is known for its potential applications in organic synthesis, particularly in the development of dyes, pharmaceuticals, and agrochemicals due to the presence of functional groups that can participate in various chemical reactions. The amino groups can act as nucleophiles, while the cyano groups can undergo reactions such as hydrolysis or reduction, making this compound versatile in synthetic chemistry. Additionally, the thiophene moiety contributes to its electronic properties, which can be beneficial in materials science. Safety data indicates that, like many nitrogen-containing compounds, it should be handled with care, as it may pose health risks upon exposure. Proper storage and handling protocols are essential to ensure safety in laboratory settings.
Formula:C6H4N4S
InChI:InChI=1S/C6H4N4S/c7-1-3-4(2-8)6(10)11-5(3)9/h9-10H2
InChI key:InChIKey=TXCXJWUMYTXWMR-UHFFFAOYSA-N
SMILES:C(#N)C=1C(C#N)=C(N)SC1N
Synonyms:
  • 2,5-Diamino-3,4-dicyanothiophene
  • 2,5-Diamino-3,4-thiophenedicarbonitrile
  • 3,4-Thiophenedicarbonitrile, 2,5-diamino-
  • NSC 409127
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