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CAS 75428-45-4

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5-Nitrothiophene-3-carboxaldehyde

Description:
5-Nitrothiophene-3-carboxaldehyde is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. The presence of a nitro group (-NO2) at the 5-position and an aldehyde group (-CHO) at the 3-position contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. This compound typically exhibits a yellow to orange color and is soluble in organic solvents. Its nitro group can participate in electrophilic substitution reactions, while the aldehyde functionality allows for further derivatization, making it a versatile intermediate in the synthesis of various chemical entities. Additionally, the compound may exhibit biological activity, which can be explored for potential pharmaceutical applications. Safety data should be consulted, as nitro compounds can be hazardous, and appropriate handling procedures should be followed. Overall, 5-Nitrothiophene-3-carboxaldehyde serves as an important building block in the development of more complex organic molecules.
Formula:C5H3NO3S
InChI:InChI=1/C5H3NO3S/c7-2-4-1-5(6(8)9)10-3-4/h1-3H
InChI key:JYVNBTUBCTXNBI-UHFFFAOYSA-N
SMILES:c1c(C=O)csc1N(=O)=O
Synonyms:
  • 2-Nitrothiophene-4-carboxaldehyde
  • 5-Nitrothiophene-3-carbaldehyde
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