
CAS 16182-15-3: Benzenesulfonic acid, 2,4,6-trimethyl-, hydrazide
Formula:C9H14N2O2S
InChI:InChI=1S/C9H14N2O2S/c1-6-4-7(2)9(8(3)5-6)14(12,13)11-10/h4-5,11H,10H2,1-3H3
InChI key:InChIKey=JQUBKTQDNVZHIY-UHFFFAOYSA-N
SMILES:S(NN)(=O)(=O)C1=C(C)C=C(C)C=C1C
Synonyms:- (2,4,6-Trimethylbenzenesulfonyl)hydrazine
- (Mesitylsulfonyl)hydrazine
- 2,4,6-Trimethylbenzene-1-sulfonohydrazide
- 2,4,6-Trimethylbenzenesulfonic acid hydrazide
- 2,4,6-Trimethylbenzenesulfonohydrazide
- 2-Mesitylenesulfonic acid, hydrazide
- 2-Mesitylenesulfonohydrazide
- Benzenesulfonic acid, 2,4,6-trimethyl-, hydrazide
- MSH
- Mesitylenesulfonic hydrazide
- Mesitylenesulfonohydrazide
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Found 6 products.
2-Mesitylenesulfonyl Hydrazide
CAS:Formula:C9H14N2O2SPurity:>97.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:214.282,4,6-Trimethylbenzenesulfonohydrazide
CAS:Controlled ProductApplications 2,4,6-Trimethylbenzenesulfonohydrazide is a reagent that generates intermediates for organic synthesis, and is applied mainly in the formation of diazine, hyrazones, Eschenmoser fragmentation and regioselective sulfonylation of pyridine/quinoline. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Wang, R., et al.: Org. Biomol. Chem., 14, 5317 (2016); Chamberlin, A. R., et al.: e-EROS Encyclopedia of Reagents for Organic Synthesis, 1 (2001)Formula:C9H14N2O2SColor and Shape:NeatMolecular weight:214.28Benzenesulfonic acid, 2,4,6-trimethyl-, hydrazide
CAS:Formula:C9H14N2O2SPurity:95%Color and Shape:SolidMolecular weight:214.28472,4,6-Trimethylbenzenesulfonohydrazide
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:214.279998779296882,4,6-Trimethylbenzenesulfonohydrazide
CAS:2,4,6-TrimethylbenzenesulfonohydrazidePurity:95%Molecular weight:214.28g/mol2,4,6-Trimethylbenzenesulfonohydrazide
CAS:2,4,6-Trimethylbenzenesulfonohydrazide is a hydrazide that has been shown to have the ability to reduce the level of vitamin D3 in the body. It binds with chloride ions and hydroxyl groups on furan rings and hydrogenates them. This reaction leads to an increase in the amount of 2,4,6-trimethylbenzenesulfonic acid (2,4,6-TMS) and a decrease in vitamin D3. The physiological activity of 2,4,6-TMS is unknown; however it has been shown to react with sodium hypochlorite to form hydroxyl radicals. Hydroxyl radicals are known for their strong oxidizing properties and can be used in medicine as antibiotics. Hydroxyl radicals also react with cyclic compounds like phenols or amines leading to alkylation reactions that may lead to DNA damage or cancer cell death.Formula:C9H14N2O2SPurity:Min. 95%Molecular weight:214.29 g/mol