5-Amino-3-chloroisoquinoline is an organic compound characterized by its isoquinoline structure, which features a bicyclic aromatic system. This compound contains an amino group (-NH2) and a chloro group (-Cl) attached to the isoquinoline ring, contributing to its reactivity and potential applications in medicinal chemistry. The presence of the amino group makes it a potential candidate for further derivatization, allowing for the synthesis of various derivatives that may exhibit biological activity. The chloro substituent can influence the compound's electronic properties and solubility, affecting its interaction with biological targets. 5-Amino-3-chloroisoquinoline is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its unique structure and functional groups make it of interest in the development of pharmaceuticals, particularly in the search for compounds with anticancer or antimicrobial properties. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis.

5-Amino-3-chloroisoquinoline

58142-49-7: 5-Amino-3-chloroisoquinoline is an organic compound characterized by its isoquinoline structure, which features a bicyclic aromatic system. This compound contains an amino group (-NH2) and a chloro group (-Cl) attached to the isoquinoline ring, contributing to its reactivity and potential applications in medicinal chemistry. The presence of the amino group makes it a potential candidate for further derivatization, allowing for the synthesis of various derivatives that may exhibit biological activity. The chloro substituent can influence the compound's electronic properties and solubility, affecting its interaction with biological targets. 5-Amino-3-chloroisoquinoline is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its unique structure and functional groups make it of interest in the development of pharmaceuticals, particularly in the search for compounds with anticancer or antimicrobial properties. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis.

CAS 58142-49-7

5-Amino-3-chloroisoquinoline

5-Amino-3-chloroisoquinoline

Ref: IN-DA00360F

3-Chloroisoquinolin-5-amine

Ref: 54-OR1004839

5-Amino-3-chloroisoquinoline

Ref: 10-F221563