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CAS 29245-44-1

:

5-Bromo-2-(5-bromo-4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-4-chloro-1,2-dihydro-3H-indol-3-one

Description:
5-Bromo-2-(5-bromo-4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-4-chloro-1,2-dihydro-3H-indol-3-one, with CAS number 29245-44-1, is a synthetic organic compound characterized by its complex indole structure, which includes multiple halogen substituents. This compound features bromine and chlorine atoms, which can significantly influence its reactivity and biological activity. The presence of the indole moiety suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as indoles are known for their diverse biological properties. The compound's structure indicates it may exhibit properties such as antimicrobial or anticancer activity, although specific biological data would be necessary to confirm these effects. Additionally, the presence of multiple halogens may enhance its lipophilicity, affecting its solubility and permeability in biological systems. As with many synthetic compounds, careful consideration of its stability, reactivity, and potential toxicity is essential for practical applications.
Formula:C16H6Br2Cl2N2O2
InChI:InChI=1S/C16H6Br2Cl2N2O2/c17-5-1-3-7-9(11(5)19)15(23)13(21-7)14-16(24)10-8(22-14)4-2-6(18)12(10)20/h1-4,21-22H
InChI key:InChIKey=FPVYDTKAOGFJJT-UHFFFAOYSA-N
SMILES:O=C1C=2C(NC1=C3C(=O)C=4C(N3)=CC=C(Br)C4Cl)=CC=C(Br)C2Cl
Synonyms:
  • Indigotin, 5,5′-dibromo-4,4′-dichloro-
  • 5-Bromo-2-(5-bromo-4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-4-chloro-1,2-dihydro-3H-indol-3-one
  • [Δ2,2′-Biindoline]-3,3′-dione, 5,5′-dibromo-4,4′-dichloro-
  • 4,4′-Dichloro-5,5′-dibromoindigo
  • 3H-Indol-3-one, 5-bromo-2-(5-bromo-4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-4-chloro-1,2-dihydro-
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