CAS 6295-94-9

N-(2-methoxyphenyl)-4-methylbenzenesulfonamide

Description:

N-(2-methoxyphenyl)-4-methylbenzenesulfonamide, with the CAS number 6295-94-9, is an organic compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. This compound features a sulfonamide moiety attached to a 4-methylbenzenesulfonyl group and a 2-methoxyphenyl group, contributing to its unique chemical structure. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the sulfonamide group. The methoxy and methyl substituents can influence its electronic properties and reactivity, potentially affecting its biological activity. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential therapeutic applications. As with many sulfonamides, it may also exhibit properties such as antibacterial activity, making it relevant in the study of antimicrobial agents. Proper handling and safety measures should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.

Formula: C₁₄H₁₅NO₃S

InChI: InChI=1/C14H15NO3S/c1-11-7-9-12(10-8-11)19(16,17)15-13-5-3-4-6-14(13)18-2/h3-10,15H,1-2H3

Synonyms:

• benzenesulfonamide, N-(2-methoxyphenyl)-4-methyl-
• N-(2-Methoxyphenyl)-4-methylbenzenesulfonamide
• N-(2-Methoxyphenyl)-p-toluenesulfonamide
• 2'-METHOXY-P-TOLUENESULFONANILIDE
• N-(2-methoxyphenyl)benzenesulfonamide4-methyl-benzenesulfonamide

N-(2-Methoxyphenyl)-4-methylbenzene-1-sulfonamide

CAS: 6295-94-9

N-(2-Methoxyphenyl)-4-methylbenzene-1-sulfonamide is a drug that has been shown to be effective in treating nerve injury. It binds to extracellular nicotinic acetylcholine receptors and blocks the neurotransmitter acetylcholine from binding to its receptor, preventing it from stimulating the postsynaptic neuron. N-(2-Methoxyphenyl)-4-methylbenzene-1-sulfonamide also prevents the release of nitric oxide, which is a neurotransmitter that stimulates the postsynaptic neuron. The dihedral angles of this compound are close to those found in natural products such as nicotine, which possess similar effects on nerve injury. This drug has been shown to be successful in treating cerebral injuries, but not peripheral ones.END>

Formula: C₁₄H₁₅NO₃S

Purity: Min. 95%

Molecular weight: 277.34 g/mol

Ref: 3D-GAA29594