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CAS 1083326-18-4

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N-(5-Bromo-3-pyridinyl)methanesulfonamide

Description:
N-(5-Bromo-3-pyridinyl)methanesulfonamide is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with a bromine atom and a methanesulfonamide functional group. The presence of the bromine atom enhances its reactivity and potential biological activity, making it of interest in medicinal chemistry. The methanesulfonamide group contributes to its solubility and stability in various solvents. This compound is typically a solid at room temperature and may exhibit moderate to high polarity due to the sulfonamide moiety. It is often utilized in research and development, particularly in the synthesis of pharmaceuticals or as a building block in organic synthesis. The compound's specific interactions, such as hydrogen bonding and potential for forming complexes, can influence its behavior in biological systems. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity.
Formula:C6H7BrN2O2S
InChI:InChI=1S/C6H7BrN2O2S/c1-12(10,11)9-6-2-5(7)3-8-4-6/h2-4,9H,1H3
InChI key:InChIKey=NGLXIPCYRBBBFC-UHFFFAOYSA-N
SMILES:N(S(C)(=O)=O)C=1C=C(Br)C=NC1
Synonyms:
  • N-(5-Bromo-3-pyridinyl)methanesulfonamide
  • Methanesulfonamide, N-(5-bromo-3-pyridinyl)-
  • 3-Bromo-5-[(methylsulfonyl)amino]pyridine
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