(1S)-1-(3-Methylphenyl)ethyl]methylamine hydrochloride, identified by its CAS number 2241594-13-6, is a chemical compound that belongs to the class of substituted amines. It features a chiral center, which contributes to its stereochemistry, specifically the (1S) configuration. The compound consists of a methylamine group attached to a 1-(3-methylphenyl)ethyl moiety, indicating the presence of a phenyl ring with a methyl substituent at the para position. This structure can influence its biological activity and interactions. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, which is advantageous for various applications, including pharmaceutical formulations. The compound may exhibit properties relevant to medicinal chemistry, potentially acting as a precursor or intermediate in the synthesis of other bioactive molecules. However, specific pharmacological effects, toxicity, and safety profiles would require further investigation through empirical studies. Overall, its unique structural features make it a compound of interest in chemical research and development.

(1S)-1-(3-METHYLPHENYL)ETHYL]METHYLAMINE HYDROCHLORIDE

2241594-13-6: (1S)-1-(3-Methylphenyl)ethyl]methylamine hydrochloride, identified by its CAS number 2241594-13-6, is a chemical compound that belongs to the class of substituted amines. It features a chiral center, which contributes to its stereochemistry, specifically the (1S) configuration. The compound consists of a methylamine group attached to a 1-(3-methylphenyl)ethyl moiety, indicating the presence of a phenyl ring with a methyl substituent at the para position. This structure can influence its biological activity and interactions. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, which is advantageous for various applications, including pharmaceutical formulations. The compound may exhibit properties relevant to medicinal chemistry, potentially acting as a precursor or intermediate in the synthesis of other bioactive molecules. However, specific pharmacological effects, toxicity, and safety profiles would require further investigation through empirical studies. Overall, its unique structural features make it a compound of interest in chemical research and development.

(S)-N-Methyl-1-(m-tolyl)ethanaminehydrochloride

<p>(S)-N-Methyl-1-(m-tolyl)ethanamine hydrochloride</p>

CAS 2241594-13-6

(1S)-1-(3-METHYLPHENYL)ETHYL]METHYLAMINE HYDROCHLORIDE

(S)-N-Methyl-1-(m-tolyl)ethanaminehydrochloride

Ref: IN-DA01KL01

(S)-N-Methyl-1-(m-tolyl)ethanamine hydrochloride

Ref: 54-OR1049664

(S)-N-Methyl-1-(m-tolyl)ethanamine hydrochloride

Ref: 10-F633711