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CAS 21889-05-4

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2-(4-Aminophenyl)indole

Description:
2-(4-Aminophenyl)indole, with the CAS number 21889-05-4, is an organic compound characterized by its indole structure fused with a phenyl group that has an amino substituent at the para position. This compound typically exhibits properties associated with both indole and aniline derivatives, including potential biological activity. It is generally a solid at room temperature and may be soluble in organic solvents, depending on the specific conditions. The presence of the amino group can impart basic characteristics, allowing it to participate in various chemical reactions, such as electrophilic substitutions or coupling reactions. Additionally, 2-(4-Aminophenyl)indole may exhibit fluorescence, making it of interest in various applications, including materials science and medicinal chemistry. Its structural features suggest potential uses in drug development, particularly in targeting specific biological pathways. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.
Formula:C14H12N2
InChI:InChI=1S/C14H12N2/c15-12-7-5-10(6-8-12)14-9-11-3-1-2-4-13(11)16-14/h1-9,16H,15H2
InChI key:InChIKey=BBYJHUAEFSHMHU-UHFFFAOYSA-N
SMILES:NC1=CC=C(C2=CC=3C(N2)=CC=CC3)C=C1
Synonyms:
  • 2-(4-Aminophenyl)indole
  • 2-(p-Aminophenyl)indole
  • 4-(1H-Indol-2-Yl)Phenylamine
  • 4-(1H-Indol-2-yl)anilin
  • 4-(1H-Indol-2-yl)benzenamine
  • Indole, 2-(p-aminophenyl)-
  • NSC 119095
  • benzenamine, 4-(1H-indol-2-yl)-
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