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CAS 1414958-76-1

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5-(5-Chloro-2-thienyl)-4-ethyl-3-isoxazolamine

Description:
5-(5-Chloro-2-thienyl)-4-ethyl-3-isoxazolamine is a chemical compound characterized by its unique structural features, which include a thienyl group, an isoxazole ring, and an amine functional group. The presence of the chloro substituent on the thienyl ring contributes to its reactivity and potential biological activity. The ethyl group enhances the lipophilicity of the molecule, which may influence its pharmacokinetic properties. This compound is likely to exhibit specific interactions with biological targets, making it of interest in medicinal chemistry and drug development. Its isoxazole moiety is known for its role in various biological activities, including anti-inflammatory and antimicrobial effects. The compound's solubility, stability, and reactivity can be influenced by the functional groups present, which are critical for its application in research or therapeutic contexts. As with many synthetic organic compounds, understanding its characteristics requires consideration of its synthesis, potential applications, and safety profile in handling and usage.
Formula:C9H9ClN2OS
InChI:InChI=1S/C9H9ClN2OS/c1-2-5-8(13-12-9(5)11)6-3-4-7(10)14-6/h3-4H,2H2,1H3,(H2,11,12)
InChI key:InChIKey=IOOWFGHLAUOHNE-UHFFFAOYSA-N
SMILES:C(C)C1=C(ON=C1N)C2=CC=C(Cl)S2
Synonyms:
  • 3-Isoxazolamine, 5-(5-chloro-2-thienyl)-4-ethyl-
  • 5-(5-Chlorothiophen-2-yl)-4-ethyl-1,2-oxazol-3-amine
  • 5-(5-Chloro-2-thienyl)-4-ethyl-3-isoxazolamine
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