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CAS 135529-19-0

:

N-[4-[[[4-[[(5-Methyl-3-isoxazolyl)amino]sulfonyl]phenyl]amino]sulfonyl]phenyl]acetamide

Description:
N-[4-[[[4-[[(5-Methyl-3-isoxazolyl)amino]sulfonyl]phenyl]amino]sulfonyl]phenyl]acetamide, with CAS number 135529-19-0, is a synthetic organic compound characterized by its complex structure, which includes multiple functional groups such as sulfonamides and an isoxazole ring. This compound typically exhibits properties associated with sulfonamide derivatives, including potential antibacterial and anti-inflammatory activities. Its molecular structure suggests it may interact with biological targets, making it of interest in pharmaceutical research. The presence of the isoxazole moiety may contribute to its biological activity, as isoxazoles are known for their diverse pharmacological properties. Additionally, the compound's solubility, stability, and reactivity can be influenced by the arrangement of its functional groups. As with many synthetic compounds, its safety profile and potential toxicity would need to be evaluated through appropriate studies. Overall, this compound represents a class of molecules that may have significant implications in medicinal chemistry and drug development.
Formula:C18H18N4O6S2
InChI:InChI=1S/C18H18N4O6S2/c1-12-11-18(20-28-12)22-30(26,27)17-9-5-15(6-10-17)21-29(24,25)16-7-3-14(4-8-16)19-13(2)23/h3-11,21H,1-2H3,(H,19,23)(H,20,22)
InChI key:InChIKey=SQPUFLYSLCMEPT-UHFFFAOYSA-N
SMILES:N(S(=O)(=O)C1=CC=C(NC(C)=O)C=C1)C2=CC=C(S(NC3=NOC(C)=C3)(=O)=O)C=C2
Synonyms:
  • N-[4-[[[4-[[(5-Methyl-3-isoxazolyl)amino]sulfonyl]phenyl]amino]sulfonyl]phenyl]acetamide
  • Acetamide, N-[4-[[[4-[[(5-methyl-3-isoxazolyl)amino]sulfonyl]phenyl]amino]sulfonyl]phenyl]-
  • Lincomycin Impurity 5 Monomer(Lincomycin EP Impurity E Monomer)
  • N-(4-Aminobenzenesulfonyl) Sulfamethoxazole N-Acetate
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