CAS 436089-20-2

N-(5-Amino-2-methylphenyl)benzenesulfonamide

Description:

N-(5-Amino-2-methylphenyl)benzenesulfonamide, also known by its CAS number 436089-20-2, is a chemical compound that belongs to the class of sulfonamides. This substance features a sulfonamide functional group (-SO2NH2) attached to a phenyl ring, which is further substituted with an amino group and a methyl group. The presence of the amino group contributes to its potential as a biological active compound, possibly exhibiting antibacterial or anti-inflammatory properties. The methyl substitution on the phenyl ring can influence the compound's solubility and reactivity. Typically, sulfonamides are known for their role in medicinal chemistry, particularly in the development of antibiotics. The compound's molecular structure suggests it may participate in hydrogen bonding due to the amino group, which can enhance its interactions with biological targets. Overall, N-(5-Amino-2-methylphenyl)benzenesulfonamide is of interest in pharmaceutical research, particularly for its potential therapeutic applications.

Formula: C₁₃H₁₄N₂O₂S

InChI: InChI=1S/C13H14N2O2S/c1-10-7-8-11(14)9-13(10)15-18(16,17)12-5-3-2-4-6-12/h2-9,15H,14H2,1H3

InChI key: InChIKey=UWSQTCSGEXESKN-UHFFFAOYSA-N

SMILES: N(S(=O)(=O)C1=CC=CC=C1)C2=C(C)C=CC(N)=C2

Synonyms:

• N-(5-Amino-2-methylphenyl)benzenesulfonamide
• Benzenesulfonamide, N-(5-amino-2-methylphenyl)-

N-(5-Amino-2-methylphenyl)benzenesulfonamide

CAS: 436089-20-2

N-(5-Amino-2-methylphenyl)benzenesulfonamide is a general inhibitor of the peptidase activity of dipeptidyl peptidase IV. This inhibitor blocks the conversion of N-terminal amino acids to their corresponding dipeptides, which prevents the formation of peptide hormones such as glucagon and insulin. It also blocks the conversion of proinsulin to insulin. N-(5-Amino-2-methylphenyl)benzenesulfonamide is used for research purposes and is not intended for therapeutic use.

Formula: C₁₃H₁₄N₂O₂S

Purity: Min. 95%

Molecular weight: 262.33 g/mol

Ref: 3D-LSA08920