CAS 176708-42-2
:N-[2-[[[3-(4-Chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-4-methoxybenzenesulfonamide
Description:
N-[2-[[[3-(4-Chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-4-methoxybenzenesulfonamide, with CAS number 176708-42-2, is a synthetic organic compound characterized by its complex structure, which includes a sulfonamide functional group, a methoxy group, and a propenyl moiety. This compound typically exhibits properties associated with sulfonamides, such as potential antibacterial activity, although its specific biological activity may vary based on its structural features. The presence of the 4-chlorophenyl group suggests possible interactions with biological targets, making it of interest in medicinal chemistry. The compound is likely to be soluble in organic solvents and may have moderate to low solubility in water, reflecting the influence of its hydrophobic aromatic components. Its molecular structure indicates potential for various chemical reactions, including substitution and coupling, which can be exploited in further synthetic applications. Overall, this compound represents a class of molecules that may have therapeutic implications, warranting further investigation into its pharmacological properties.
Formula:C24H25ClN2O3S
InChI:InChI=1S/C24H25ClN2O3S/c1-27(17-5-6-19-9-11-21(25)12-10-19)18-20-7-3-4-8-24(20)26-31(28,29)23-15-13-22(30-2)14-16-23/h3-16,26H,17-18H2,1-2H3
InChI key:InChIKey=RUAOVVIUGUOYHA-UHFFFAOYSA-N
SMILES:N(S(=O)(=O)C1=CC=C(OC)C=C1)C2=C(CN(CC=CC3=CC=C(Cl)C=C3)C)C=CC=C2
Synonyms:- N-[2-[[[3-(4-Chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-4-methoxybenzenesulfonamide
- Benzenesulfonamide, N-[2-[[[3-(4-chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-4-methoxy-
- KN 92
- Benzenesulfonamide, N-[2-[[[3-(4-chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-4-methoxy-
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Found 3 products.
KN-92
CAS:<p>KN-92 is an inactive analog of the CaM kinase II inhibitor KN 93.</p>Formula:C24H25ClN2O3SColor and Shape:SolidMolecular weight:456.98KN-92
CAS:<p>KN-92 is a potassium channel opener that has been shown to increase intracellular calcium levels in cardiac and neuronal cells. It also increases the energy metabolism of cardiac cells by increasing the mitochondrial membrane potential, leading to increased production of ATP. KN-92 has been shown to be effective in experimental models for structural heart disease. It also reduces the incidence of atrial arrhythmia and congestive heart failure in rats with experimentally induced myocardial infarction. KN-92 is not active against granule neurons.</p>Formula:C24H25ClN2O3SPurity:Min. 95%Molecular weight:456.98 g/mol


