3-(2,3-Dichlorophenoxy)-N-(2-hydroxyethyl)propan-1-aminium, with the CAS number 418788-90-6, is a quaternary ammonium compound characterized by its cationic nature due to the presence of a positively charged nitrogen atom. This compound features a propan-1-aminium backbone, which is substituted with a 2,3-dichlorophenoxy group and a hydroxyethyl group, contributing to its unique chemical properties. The dichlorophenoxy moiety enhances its hydrophobic characteristics, while the hydroxyethyl group increases its solubility in polar solvents. This compound is likely to exhibit antimicrobial properties, making it of interest in various applications, including disinfectants and surfactants. Its quaternary structure may also impart stability and effectiveness in biological systems. Additionally, the presence of chlorine atoms can influence its reactivity and interaction with biological membranes. Overall, this compound's structural features suggest potential utility in both industrial and pharmaceutical contexts, although specific applications would depend on further research and testing.

3-(2,3-dichlorophenoxy)-N-(2-hydroxyethyl)propan-1-aminium

418788-90-6: 3-(2,3-Dichlorophenoxy)-N-(2-hydroxyethyl)propan-1-aminium, with the CAS number 418788-90-6, is a quaternary ammonium compound characterized by its cationic nature due to the presence of a positively charged nitrogen atom. This compound features a propan-1-aminium backbone, which is substituted with a 2,3-dichlorophenoxy group and a hydroxyethyl group, contributing to its unique chemical properties. The dichlorophenoxy moiety enhances its hydrophobic characteristics, while the hydroxyethyl group increases its solubility in polar solvents. This compound is likely to exhibit antimicrobial properties, making it of interest in various applications, including disinfectants and surfactants. Its quaternary structure may also impart stability and effectiveness in biological systems. Additionally, the presence of chlorine atoms can influence its reactivity and interaction with biological membranes. Overall, this compound's structural features suggest potential utility in both industrial and pharmaceutical contexts, although specific applications would depend on further research and testing.

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2-(3-(2,3-Dichlorophenoxy)propylamino)ethanol hydrochloride

Induces p21, S-phase arrest in cancer cells through ERK pathways. IC50: 0.89 μM (LoVo cells), 12.6 μM (fibroblasts).

CAS 418788-90-6

3-(2,3-dichlorophenoxy)-N-(2-hydroxyethyl)propan-1-aminium

2-(3-(2,3-Dichlorophenoxy)propylamino)ethanol hydrochloride

Ref: 02-J64981

2,3-DCPE

Ref: TM-T22490