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CAS 4403-78-5

:

N,N′-1,2-Ethanediylbis[4-methylbenzenesulfonamide]

Description:
N,N′-1,2-Ethanediylbis[4-methylbenzenesulfonamide], with the CAS number 4403-78-5, is an organic compound characterized by its sulfonamide functional groups attached to a central ethanediyl (ethylene) bridge. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents, such as water and alcohols, due to the presence of sulfonamide groups, which enhance its hydrophilicity. The sulfonamide moieties contribute to its potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its structure allows for various interactions, including hydrogen bonding and dipole-dipole interactions, which can influence its reactivity and solubility. Additionally, the presence of the methyl groups on the aromatic rings can affect its electronic properties and steric hindrance, impacting its biological activity and interactions with other molecules. Overall, this compound's unique structural features make it a subject of interest in both synthetic and medicinal chemistry.
Formula:C16H20N2O4S2
InChI:InChI=1/C16H20N2O4S2/c1-13-3-7-15(8-4-13)23(19,20)17-11-12-18-24(21,22)16-9-5-14(2)6-10-16/h3-10,17-18H,11-12H2,1-2H3
InChI key:InChIKey=HOFGETLODCEHBQ-UHFFFAOYSA-N
SMILES:S(NCCNS(=O)(=O)C1=CC=C(C)C=C1)(=O)(=O)C2=CC=C(C)C=C2
Synonyms:
  • 1,2-(Tosylamino)ethane
  • N,N′-(Ethane-1,2-diyl)bis(4-methylbenzenesulfonamide)
  • N,N′-1,2-Ethanediylbis[4-methylbenzenesulfonamide]
  • N,N′-Bis(p-toluenesulfonyl)ethylenediamine
  • N,N′-Bis(p-tolylsulfonyl)-1,2-ethylenediamine
  • N,N′-Bis(toluenesulfonyl)-1,2-ethylenediamine
  • N,N′-Bis(tosyl)-1,2-diaminoethane
  • N,N′-Ditosylethylenediamine
  • N,N′-Ethylenebis(p-toluenesulfonamide)
  • NSC 25018
  • See more synonyms
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