7-Hydroxy-2,3(1H)-Isoquinolinedicarboxylic acid, 3,4-dihydro-2-(1,1-dimethylethyl) ester, with CAS number 183158-78-3, is a chemical compound characterized by its isoquinoline structure, which is a bicyclic compound containing a fused benzene and pyridine ring. This compound features two carboxylic acid groups, which contribute to its acidity and potential for forming salts or esters. The presence of a hydroxyl group enhances its polarity and solubility in polar solvents. The ester functionality, derived from the reaction of the carboxylic acid with an alcohol, suggests that this compound may exhibit different physical and chemical properties compared to its acid form, such as improved lipophilicity. The tert-butyl group (1,1-dimethylethyl) attached to the ester may provide steric hindrance, influencing its reactivity and interactions with biological targets. Overall, this compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological systems.

7-hydroxy-2,3(1H)-Isoquinolinedicarboxylic acid, 3,4-dihydro- 2-(1,1-dimethylethyl) ester

183158-78-3: 7-Hydroxy-2,3(1H)-Isoquinolinedicarboxylic acid, 3,4-dihydro-2-(1,1-dimethylethyl) ester, with CAS number 183158-78-3, is a chemical compound characterized by its isoquinoline structure, which is a bicyclic compound containing a fused benzene and pyridine ring. This compound features two carboxylic acid groups, which contribute to its acidity and potential for forming salts or esters. The presence of a hydroxyl group enhances its polarity and solubility in polar solvents. The ester functionality, derived from the reaction of the carboxylic acid with an alcohol, suggests that this compound may exhibit different physical and chemical properties compared to its acid form, such as improved lipophilicity. The tert-butyl group (1,1-dimethylethyl) attached to the ester may provide steric hindrance, influencing its reactivity and interactions with biological targets. Overall, this compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological systems.

<p>2-(tert-Butoxycarbonyl)-7-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid</p>

CAS 183158-78-3

7-hydroxy-2,3(1H)-Isoquinolinedicarboxylic acid, 3,4-dihydro- 2-(1,1-dimethylethyl) ester

2-(tert-Butoxycarbonyl)-7-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Ref: 54-OR1032544

2-(TERT-BUTOXYCARBONYL)-7-HYDROXY-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

Ref: 10-F839280