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CAS 5429-62-9

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Ethyl 2-(1H-benzimidazol-2-ylthio)acetate

Description:
Ethyl 2-(1H-benzimidazol-2-ylthio)acetate is an organic compound characterized by its benzimidazole moiety, which contributes to its biological activity and potential applications in pharmaceuticals. The compound features an ethyl ester functional group, which enhances its solubility and reactivity. Its structure includes a thioether linkage, which can influence its chemical properties and interactions. Ethyl 2-(1H-benzimidazol-2-ylthio)acetate is typically a solid or liquid at room temperature, depending on its purity and specific formulation. It may exhibit moderate to high stability under standard conditions, but like many organic compounds, it should be handled with care to avoid degradation or unwanted reactions. The compound's unique structure suggests potential applications in medicinal chemistry, particularly in the development of anti-parasitic or anti-cancer agents, due to the biological significance of benzimidazole derivatives. As with any chemical substance, proper safety protocols should be followed when handling it in a laboratory setting.
Formula:C11H12N2O2S
InChI:InChI=1S/C11H12N2O2S/c1-2-15-10(14)7-16-11-12-8-5-3-4-6-9(8)13-11/h3-6H,2,7H2,1H3,(H,12,13)
InChI key:InChIKey=TZMSMSYMMHOSOE-UHFFFAOYSA-N
SMILES:S(CC(OCC)=O)C=1NC=2C(N1)=CC=CC2
Synonyms:
  • (1H-Benzoimidazol-2-ylsulfanyl)-acetic acid ethyl ester
  • Acetic acid, (1H-benzimidazol-2-ylthio)-, ethyl ester
  • Acetic acid, (2-benzimidazolylthio)-, ethyl ester
  • Acetic acid, 2-(1H-benzimidazol-2-ylthio)-, ethyl ester
  • Ethyl 2-(1H-benzimidazol-2-ylthio)acetate
  • Ethyl 2-(2-benzimidazolylthio)acetate
  • NSC 14189
  • [(1H-Benzimidazol-2-yl)sulfanyl]acetic acid ethyl ester
  • ethyl (1H-benzimidazol-2-ylthio)acetate
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