6-Chloro-1,2,3,4-tetrahydroquinoxaline is a heterocyclic organic compound characterized by its bicyclic structure, which includes a quinoxaline framework with a chlorine substituent at the 6-position. This compound is typically a colorless to pale yellow solid and is soluble in organic solvents. Its molecular structure features a saturated tetrahydroquinoxaline ring, which contributes to its unique chemical reactivity and potential biological activity. The presence of the chlorine atom can influence its electronic properties and reactivity, making it a subject of interest in medicinal chemistry and drug development. 6-Chloro-1,2,3,4-tetrahydroquinoxaline may exhibit various pharmacological activities, including potential neuroprotective or anti-inflammatory effects, although specific biological data may vary. As with many heterocycles, it can participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, making it a versatile building block in organic synthesis. Proper handling and safety measures should be observed due to its chemical nature and potential biological effects.

6-chloro-1,2,3,4-tetrahydroquinoxaline

73855-45-5: 6-Chloro-1,2,3,4-tetrahydroquinoxaline is a heterocyclic organic compound characterized by its bicyclic structure, which includes a quinoxaline framework with a chlorine substituent at the 6-position. This compound is typically a colorless to pale yellow solid and is soluble in organic solvents. Its molecular structure features a saturated tetrahydroquinoxaline ring, which contributes to its unique chemical reactivity and potential biological activity. The presence of the chlorine atom can influence its electronic properties and reactivity, making it a subject of interest in medicinal chemistry and drug development. 6-Chloro-1,2,3,4-tetrahydroquinoxaline may exhibit various pharmacological activities, including potential neuroprotective or anti-inflammatory effects, although specific biological data may vary. As with many heterocycles, it can participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, making it a versatile building block in organic synthesis. Proper handling and safety measures should be observed due to its chemical nature and potential biological effects.

CAS 73855-45-5

6-chloro-1,2,3,4-tetrahydroquinoxaline

6-Chloro-1,2,3,4-tetrahydro-quinoxaline

Ref: IN-DA00FCZ3