Methyl 2-([(4-methylphenyl)sulfonyl]methyl)-3-nitrobenzenecarboxylate, identified by its CAS number 860786-92-1, is a chemical compound characterized by its complex structure, which includes a methyl ester functional group, a nitro group, and a sulfonyl moiety. This compound typically exhibits properties associated with aromatic compounds, such as stability and potential for electrophilic substitution reactions due to the presence of the nitro group, which is a strong electron-withdrawing group. The sulfonyl group enhances the compound's solubility in polar solvents and may influence its reactivity and biological activity. Methyl esters are generally known for their pleasant odors and are often used in organic synthesis and as intermediates in the production of pharmaceuticals. The presence of the 4-methylphenyl group may impart additional hydrophobic characteristics, affecting the compound's interaction with biological systems. Overall, this compound's unique functional groups suggest potential applications in medicinal chemistry and materials science, although specific biological activities and reactivity would require further investigation.

METHYL 2-([(4-METHYLPHENYL)SULFONYL]METHYL)-3-NITROBENZENECARBOXYLATE

860786-92-1: Methyl 2-([(4-methylphenyl)sulfonyl]methyl)-3-nitrobenzenecarboxylate, identified by its CAS number 860786-92-1, is a chemical compound characterized by its complex structure, which includes a methyl ester functional group, a nitro group, and a sulfonyl moiety. This compound typically exhibits properties associated with aromatic compounds, such as stability and potential for electrophilic substitution reactions due to the presence of the nitro group, which is a strong electron-withdrawing group. The sulfonyl group enhances the compound's solubility in polar solvents and may influence its reactivity and biological activity. Methyl esters are generally known for their pleasant odors and are often used in organic synthesis and as intermediates in the production of pharmaceuticals. The presence of the 4-methylphenyl group may impart additional hydrophobic characteristics, affecting the compound's interaction with biological systems. Overall, this compound's unique functional groups suggest potential applications in medicinal chemistry and materials science, although specific biological activities and reactivity would require further investigation.

CAS 860786-92-1

METHYL 2-([(4-METHYLPHENYL)SULFONYL]METHYL)-3-NITROBENZENECARBOXYLATE