1,2,3,4-Tetrahydroisoquinoline-4,6-diol is a bicyclic organic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. This compound features a tetrahydro configuration, indicating the presence of four hydrogen atoms that saturate the ring system, resulting in a more stable structure compared to its unsaturated counterparts. The presence of hydroxyl (-OH) groups at the 4 and 6 positions contributes to its potential as a versatile building block in organic synthesis and medicinal chemistry. These hydroxyl groups can participate in hydrogen bonding, influencing the compound's solubility and reactivity. The compound is of interest in various fields, including pharmacology, due to its potential biological activities, which may include neuroprotective and anti-inflammatory effects. Its molecular structure allows for various modifications, making it a candidate for further research in drug development. As with many organic compounds, its physical properties, such as melting point and solubility, can vary based on environmental conditions and the presence of other substances.

1,2,3,4-tetrahydroisoquinoline-4,6-diol

93202-93-8: 1,2,3,4-Tetrahydroisoquinoline-4,6-diol is a bicyclic organic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. This compound features a tetrahydro configuration, indicating the presence of four hydrogen atoms that saturate the ring system, resulting in a more stable structure compared to its unsaturated counterparts. The presence of hydroxyl (-OH) groups at the 4 and 6 positions contributes to its potential as a versatile building block in organic synthesis and medicinal chemistry. These hydroxyl groups can participate in hydrogen bonding, influencing the compound's solubility and reactivity. The compound is of interest in various fields, including pharmacology, due to its potential biological activities, which may include neuroprotective and anti-inflammatory effects. Its molecular structure allows for various modifications, making it a candidate for further research in drug development. As with many organic compounds, its physical properties, such as melting point and solubility, can vary based on environmental conditions and the presence of other substances.

CAS 93202-93-8

1,2,3,4-tetrahydroisoquinoline-4,6-diol

1,2,3,4-Tetrahydroisoquinoline-4,6-diol

Ref: IN-DA006I14

1,2,3,4-Tetrahydroisoquinoline-4,6-diol

Ref: 54-OR86911

1,2,3,4-Tetrahydroisoquinoline-4,6-diol

Ref: 10-F779982