CAS 179246-08-3
:4-Quinolinamine, 6,7-dimethoxy-N-(3-phenoxyphenyl)-,monohydrochloride
Description:
4-Quinolinamine, 6,7-dimethoxy-N-(3-phenoxyphenyl)-, monohydrochloride, identified by CAS number 179246-08-3, is a chemical compound that belongs to the class of quinoline derivatives. This substance features a quinoline core, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. The presence of methoxy groups at the 6 and 7 positions enhances its lipophilicity and may influence its biological activity. The N-(3-phenoxyphenyl) substituent suggests potential interactions with various biological targets, making it of interest in medicinal chemistry. As a hydrochloride salt, it is typically more soluble in water than its free base form, which can facilitate its use in pharmaceutical formulations. The compound may exhibit various pharmacological properties, including potential antitumor or antimicrobial activities, although specific biological effects would require further investigation. Safety and handling precautions should be observed, as with any chemical substance, particularly in laboratory settings.
Formula:C23H20N2O3・ClH
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Found 5 products.
6,7-Dimethoxy-N-(3-phenoxyphenyl)quinolin-4-amine hydrochloride
CAS:Formula:C23H21ClN2O3Purity:95%Color and Shape:SolidMolecular weight:408.8774GW 284543 hydrochloride
CAS:<p>GW 284543 hydrochloride is a selective inhibitor of MEK5 .</p>Formula:C23H21ClN2O3Purity:99.73%Color and Shape:SolidMolecular weight:408.876,7-Dimethoxy-N-(3-phenoxyphenyl)quinolin-4-amine hydrochloride
CAS:Formula:C23H21ClN2O3Purity:95%Molecular weight:408.886,7-Dimethoxy-N-(3-phenoxyphenyl)quinolin-4-amine hydrochloride
CAS:<p>6,7-Dimethoxy-N-(3-phenoxyphenyl)quinolin-4-amine hydrochloride is an inhibitor of the N-methyl-D-aspartate receptor, which regulates synaptic transmission. This drug was developed as a research tool to study the function of ion channels and receptors.</p>Formula:C23H21ClN2O3Purity:Min. 95%Molecular weight:408.9 g/mol





