(3S)-1,2,3,4-Tetrahydroquinolin-3-ol is a bicyclic organic compound characterized by its tetrahydroquinoline structure, which consists of a fused benzene and piperidine ring. The "3S" designation indicates that the compound has a specific stereochemistry at the carbon atom in the 3-position, which is crucial for its biological activity. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents and may exhibit limited solubility in water. The presence of the hydroxyl (-OH) group contributes to its potential as a hydrogen bond donor, influencing its reactivity and interactions with other molecules. (3S)-1,2,3,4-Tetrahydroquinolin-3-ol has garnered interest in medicinal chemistry due to its potential pharmacological properties, including neuroprotective and anti-inflammatory effects. Its unique structure allows for various modifications, making it a valuable scaffold in drug design and development. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with exposure.

(3S)-1,2,3,4-TETRAHYDROQUINOLIN-3-OL

206563-20-4: (3S)-1,2,3,4-Tetrahydroquinolin-3-ol is a bicyclic organic compound characterized by its tetrahydroquinoline structure, which consists of a fused benzene and piperidine ring. The "3S" designation indicates that the compound has a specific stereochemistry at the carbon atom in the 3-position, which is crucial for its biological activity. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents and may exhibit limited solubility in water. The presence of the hydroxyl (-OH) group contributes to its potential as a hydrogen bond donor, influencing its reactivity and interactions with other molecules. (3S)-1,2,3,4-Tetrahydroquinolin-3-ol has garnered interest in medicinal chemistry due to its potential pharmacological properties, including neuroprotective and anti-inflammatory effects. Its unique structure allows for various modifications, making it a valuable scaffold in drug design and development. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with exposure.

CAS 206563-20-4

(3S)-1,2,3,4-TETRAHYDROQUINOLIN-3-OL

3-Quinolinol, 1,2,3,4-tetrahydro-, (3S)-

Ref: IN-DA00IL7T

(3S)-1,2,3,4-tetrahydroquinolin-3-ol

Ref: 10-F519918