CAS 4543-58-2
:2,4,6-Trimethylbenzenesulfonamide
Description:
2,4,6-Trimethylbenzenesulfonamide, with the CAS number 4543-58-2, is an organic compound characterized by its sulfonamide functional group attached to a trimethyl-substituted benzene ring. This compound typically appears as a solid at room temperature and is soluble in polar organic solvents. The presence of the sulfonamide group imparts unique chemical properties, including the ability to participate in hydrogen bonding, which can influence its reactivity and interactions with biological systems. 2,4,6-Trimethylbenzenesulfonamide may exhibit moderate to high stability under standard conditions, but it can be sensitive to strong acids or bases. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as a reagent in organic synthesis. Additionally, the trimethyl groups contribute to steric hindrance, which can affect the compound's reactivity and interactions with other molecules. Safety data should be consulted for handling and exposure guidelines, as sulfonamides can have varying biological effects.
Formula:C9H13NO2S
InChI:InChI=1/C9H13NO2S/c1-6-4-7(2)9(8(3)5-6)13(10,11)12/h4-5H,1-3H3,(H2,10,11,12)
InChI key:InChIKey=YECJUZIGFPJWGQ-UHFFFAOYSA-N
SMILES:S(N)(=O)(=O)C1=C(C)C=C(C)C=C1C
Synonyms:- 2,4,6-Trimethylbenzene-1-sulfonamide
- 2-Mesitylenesulfonamide
- Benzenesulfonamide, 2,4,6-Trimethyl-
- Mesitylenesulfonamide
- Mesitylsulfonamide
- NSC 87569
- 2,4,6-Trimethylbenzenesulfonamide
- SKL393
- Benzenesulfonamide, 2,4,6-trimethyl- (9CI)
- Mesitylene-2-sulphonamide, 2-Sulphamoylmesitylene
- 2,4,6-Trimethylbenzenesulfonamid
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Found 4 products.
2,4,6-Trimethylbenzenesulfonamide
CAS:Formula:C9H13NO2SPurity:96%Color and Shape:SolidMolecular weight:199.27002,4,6-Trimethylbenzenesulphonamide
CAS:2,4,6-TrimethylbenzenesulphonamidePurity:≥95%Color and Shape:SolidMolecular weight:199.27g/mol2,4,6-Trimethylbenzenesulfonamide
CAS:<p>2,4,6-Trimethylbenzenesulfonamide is an organic solvent that has a range of uses in the manufacture of plastics and elastomers. It also has inflammatory properties and may be used to induce symptoms of dermatitis. This compound competitively inhibits the production of imine from amino acid precursors and reactive oxygen species (ROS) formation by neutrophils. 2,4,6-Trimethylbenzenesulfonamide has been shown to have antibacterial activity against thp-1 cells and chloride ion channels. The inhibitory properties of this compound are due to its ability to interfere with the transepidermal water loss (TEWL).</p>Formula:C9H13NO2SPurity:Min. 95%Molecular weight:199.27 g/mol



