
CAS 2644-99-7
:{methyl[(4-methylphenyl)sulfonyl]amino}acetate
Description:
Methyl[(4-methylphenyl)sulfonyl]aminoacetate, with the CAS number 2644-99-7, is an organic compound characterized by its sulfonamide functional group and an acetate moiety. This compound features a methyl group attached to a phenyl ring that has a methyl substituent at the para position, contributing to its hydrophobic characteristics. The sulfonyl group enhances the compound's reactivity and solubility in polar solvents, while the aminoacetate portion provides basic properties. Typically, compounds of this nature exhibit moderate to high stability under standard conditions but may be sensitive to strong acids or bases. They can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making them valuable in synthetic organic chemistry. Additionally, the presence of the sulfonyl group often imparts unique biological activities, which may be explored in pharmaceutical applications. Overall, methyl[(4-methylphenyl)sulfonyl]aminoacetate is a versatile compound with potential utility in both research and industrial settings.
Formula:C10H12NO4S
InChI:InChI=1/C10H13NO4S/c1-8-3-5-9(6-4-8)16(14,15)11(2)7-10(12)13/h3-6H,7H2,1-2H3,(H,12,13)/p-1
SMILES:Cc1ccc(cc1)S(=O)(=O)N(C)CC(=O)[O-]
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Found 3 products.
Tosylsarcosine-13C3
CAS:Controlled ProductFormula:C7H16N2Color and Shape:NeatMolecular weight:128.2152-(N-Methyl4-methylbenzenesulfonamido)acetic acid
CAS:2-(N-Methy4-methylbenzenesulfonamido)acetic acid is a chiral amide that can be used to prepare enantiomerically enriched olefins. It is used in the asymmetric acylation of olefins and has been shown to form cyclobutanones with high stereoselectivity. 2-(N-Methyl4-methylbenzenesulfonamido)acetic acid can also be used for the preparation of vicinal adducts and hydrolysis products of this compound.Formula:C10H13NO4SPurity:Min. 95%Molecular weight:243.28 g/mol


