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CAS 38401-68-2

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5-(4-Methylphenyl)-2-thiophenecarboxaldehyde

Description:
5-(4-Methylphenyl)-2-thiophenecarboxaldehyde is an organic compound characterized by its unique structure, which includes a thiophene ring and an aldehyde functional group. The presence of the 4-methylphenyl group enhances its aromatic properties, contributing to its stability and reactivity. This compound typically appears as a yellow to brown liquid or solid, depending on its purity and specific conditions. It is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, such as nucleophilic additions and condensation reactions. The thiophene moiety can also impart interesting electronic properties, making it a subject of interest in materials science and organic electronics. Additionally, like many aldehydes, it may exhibit characteristic odors and can be reactive towards nucleophiles, making it a versatile building block in synthetic chemistry. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C12H10OS
InChI:InChI=1S/C12H10OS/c1-9-2-4-10(5-3-9)12-7-6-11(8-13)14-12/h2-8H,1H3
InChI key:InChIKey=CNHGZKBPLKLVSD-UHFFFAOYSA-N
SMILES:C(=O)C=1SC(=CC1)C2=CC=C(C)C=C2
Synonyms:
  • 2-Thiophenecarboxaldehyde, 5-(4-methylphenyl)-
  • 5-p-Tolyl-2-thiophenecarboxaldehyde
  • 5-(4-Methylphenyl)-2-thiophenecarboxaldehyde
  • 2-Formyl-5-(4-methylphenyl)thiophene
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