5-Bromoisoquinoline-1-carboxylic acid is a heterocyclic organic compound characterized by its isoquinoline structure, which features a fused benzene and pyridine ring system. The presence of a bromine atom at the 5-position and a carboxylic acid functional group at the 1-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar organic solvents. It exhibits acidic behavior due to the carboxylic acid group, which can participate in hydrogen bonding and influence its reactivity. The bromine substituent can also serve as a site for further chemical modifications, making it a valuable intermediate in organic synthesis and medicinal chemistry. Additionally, compounds like 5-bromoisoquinoline-1-carboxylic acid may exhibit biological activity, which can be explored for potential pharmaceutical applications. Its molecular structure and functional groups allow for various reactions, including nucleophilic substitutions and coupling reactions, making it a versatile compound in synthetic organic chemistry.

5-bromoisoquinoline-1-carboxylic acid

1111311-65-9: 5-Bromoisoquinoline-1-carboxylic acid is a heterocyclic organic compound characterized by its isoquinoline structure, which features a fused benzene and pyridine ring system. The presence of a bromine atom at the 5-position and a carboxylic acid functional group at the 1-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar organic solvents. It exhibits acidic behavior due to the carboxylic acid group, which can participate in hydrogen bonding and influence its reactivity. The bromine substituent can also serve as a site for further chemical modifications, making it a valuable intermediate in organic synthesis and medicinal chemistry. Additionally, compounds like 5-bromoisoquinoline-1-carboxylic acid may exhibit biological activity, which can be explored for potential pharmaceutical applications. Its molecular structure and functional groups allow for various reactions, including nucleophilic substitutions and coupling reactions, making it a versatile compound in synthetic organic chemistry.

CAS 1111311-65-9

5-bromoisoquinoline-1-carboxylic acid

5-Bromoisoquinoline-1-carboxylic acid

Ref: IN-DA00926I

Ethyl 5-Bromoisoquinoline-1-carboxylate

Ref: 54-OR470933