2-(3-Chloro-4-methoxyphenyl)ethanamine hydrochloride, with the CAS number 7569-60-0, is a chemical compound characterized by its amine functional group and aromatic structure. This substance features a chloro and methoxy substituent on a phenyl ring, which influences its chemical reactivity and biological activity. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in various applications, particularly in pharmaceuticals. The presence of the chloro group can affect the compound's electronic properties, while the methoxy group may contribute to its lipophilicity. This compound is often studied for its potential pharmacological effects, including its role as a precursor or intermediate in the synthesis of other bioactive molecules. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper laboratory practices are followed. Overall, its unique structural features make it a subject of interest in medicinal chemistry and related fields.

2-(3-chloro-4-methoxyphenyl)ethanamine hydrochloride

7569-60-0: 2-(3-Chloro-4-methoxyphenyl)ethanamine hydrochloride, with the CAS number 7569-60-0, is a chemical compound characterized by its amine functional group and aromatic structure. This substance features a chloro and methoxy substituent on a phenyl ring, which influences its chemical reactivity and biological activity. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in various applications, particularly in pharmaceuticals. The presence of the chloro group can affect the compound's electronic properties, while the methoxy group may contribute to its lipophilicity. This compound is often studied for its potential pharmacological effects, including its role as a precursor or intermediate in the synthesis of other bioactive molecules. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper laboratory practices are followed. Overall, its unique structural features make it a subject of interest in medicinal chemistry and related fields.

2-(3-Chloro-4-methoxyphenyl)ethylamine hydrochloride

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CAS 7569-60-0

2-(3-chloro-4-methoxyphenyl)ethanamine hydrochloride

2-(3-Chloro-4-methoxyphenyl)ethylamine hydrochloride

Ref: IN-DA003J8G

2-(3-Chloro-4-methoxyphenyl)ethan-1-amine hydrochloride

Ref: 3D-HAA56960