CAS 353502-16-6

N-(3,5-Dimethylphenyl)-N-(methylsulfonyl)glycine

Description:

N-(3,5-Dimethylphenyl)-N-(methylsulfonyl)glycine, identified by its CAS number 353502-16-6, is an organic compound characterized by its unique molecular structure, which includes a glycine backbone substituted with a 3,5-dimethylphenyl group and a methylsulfonyl moiety. This compound typically exhibits properties associated with amino acids, such as being polar and potentially soluble in water, depending on the specific conditions. The presence of the methylsulfonyl group may impart additional characteristics, such as increased stability and potential for interaction with biological systems. It may also exhibit biological activity, making it of interest in pharmaceutical research. The compound's molecular interactions can be influenced by its functional groups, which may affect its reactivity and binding affinity in various chemical and biological contexts. Overall, N-(3,5-Dimethylphenyl)-N-(methylsulfonyl)glycine represents a class of compounds that could have applications in medicinal chemistry and drug development.

Formula: C₁₁H₁₅NO₄S

InChI: InChI=1S/C11H15NO4S/c1-8-4-9(2)6-10(5-8)12(7-11(13)14)17(3,15)16/h4-6H,7H2,1-3H3,(H,13,14)

InChI key: InChIKey=OQUXVZYPPBRNBL-UHFFFAOYSA-N

SMILES: N(CC(O)=O)(S(C)(=O)=O)C1=CC(C)=CC(C)=C1

Synonyms:

• Glycine, N-(3,5-dimethylphenyl)-N-(methylsulfonyl)-
• N-(3,5-Dimethylphenyl)-N-(methylsulfonyl)glycine
• [(3,5-Dimethyl-phenyl)-methanesulfonyl-amino]-acetic acid
• 2-[(3,5-dimethylphenyl)-methylsulfonyl-amino]acetic acid
• 2-[(3,5-dimethylphenyl)-mesyl-amino]acetic acid
• 2-[(3,5-dimethylphenyl)-methylsulfonylamino]acetic acid
• 2-[(3,5-dimethylphenyl)-methylsulfonyl-amino]ethanoic acid