(R)-(+)-1-(4-Methoxyphenyl)ethylamine hydrochloride, with the CAS number 911373-69-8, is a chiral amine characterized by its specific stereochemistry, which is crucial for its biological activity. This compound features a phenyl ring substituted with a methoxy group at the para position, contributing to its lipophilicity and potential interactions with biological targets. The presence of the ethylamine moiety suggests it may participate in hydrogen bonding and ionic interactions, enhancing its solubility in polar solvents. As a hydrochloride salt, it is typically more stable and soluble in aqueous solutions compared to its free base form. This compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting the central nervous system or other therapeutic areas, due to its potential to interact with neurotransmitter systems. Its chiral nature implies that the (R)-enantiomer may exhibit different pharmacological properties compared to its (S)-counterpart, making stereochemical considerations essential in its application and study.

(R)-(+)-1-(4-Methoxyphenyl)Ethylamine-Hcl

911373-69-8: (R)-(+)-1-(4-Methoxyphenyl)ethylamine hydrochloride, with the CAS number 911373-69-8, is a chiral amine characterized by its specific stereochemistry, which is crucial for its biological activity. This compound features a phenyl ring substituted with a methoxy group at the para position, contributing to its lipophilicity and potential interactions with biological targets. The presence of the ethylamine moiety suggests it may participate in hydrogen bonding and ionic interactions, enhancing its solubility in polar solvents. As a hydrochloride salt, it is typically more stable and soluble in aqueous solutions compared to its free base form. This compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting the central nervous system or other therapeutic areas, due to its potential to interact with neurotransmitter systems. Its chiral nature implies that the (R)-enantiomer may exhibit different pharmacological properties compared to its (S)-counterpart, making stereochemical considerations essential in its application and study.

(R)-(+)-1-(4-METHOXYPHENYL)ETHYLAMINE-HCl

(R)-(+)-1-(4-Methoxyphenyl)ethylamine-HCl

CAS 911373-69-8

(R)-(+)-1-(4-Methoxyphenyl)Ethylamine-Hcl

(R)-(+)-1-(4-METHOXYPHENYL)ETHYLAMINE-HCl

Ref: IN-DA00H0F3

(R)-(+)-1-(4-Methoxyphenyl)ethylamine-HCl

Ref: 54-OR1043107

(R)-(+)-1-(4-Methoxyphenyl)ethylamine hydrochloride

Ref: 10-F210022