1-Chloropyrido[3,4-d]pyridazine is a heterocyclic compound characterized by its fused pyridine and pyridazine rings, with a chlorine substituent at the 1-position of the pyridine ring. This compound typically exhibits a pale to light yellow appearance and is soluble in organic solvents. Its molecular structure contributes to its potential biological activity, making it of interest in medicinal chemistry and pharmaceutical research. The presence of the chlorine atom can influence its reactivity and interaction with biological targets. Additionally, the compound may exhibit properties such as moderate stability under standard conditions, but it may be sensitive to strong acids or bases. Its synthesis often involves multi-step reactions, and it may serve as an intermediate in the development of more complex molecules. As with many heterocycles, it may also display interesting electronic properties due to the arrangement of nitrogen atoms within the ring system, which can affect its behavior in various chemical reactions. Safety data should be consulted for handling and storage, as with any chemical substance.

1-CHLOROPYRIDO[3,4-D]PYRIDAZINE

162022-92-6: 1-Chloropyrido[3,4-d]pyridazine is a heterocyclic compound characterized by its fused pyridine and pyridazine rings, with a chlorine substituent at the 1-position of the pyridine ring. This compound typically exhibits a pale to light yellow appearance and is soluble in organic solvents. Its molecular structure contributes to its potential biological activity, making it of interest in medicinal chemistry and pharmaceutical research. The presence of the chlorine atom can influence its reactivity and interaction with biological targets. Additionally, the compound may exhibit properties such as moderate stability under standard conditions, but it may be sensitive to strong acids or bases. Its synthesis often involves multi-step reactions, and it may serve as an intermediate in the development of more complex molecules. As with many heterocycles, it may also display interesting electronic properties due to the arrangement of nitrogen atoms within the ring system, which can affect its behavior in various chemical reactions. Safety data should be consulted for handling and storage, as with any chemical substance.

CAS 162022-92-6

1-CHLOROPYRIDO[3,4-D]PYRIDAZINE

1-CHLOROPYRIDO[3,4-D]PYRIDAZINE

Ref: IN-DA001SND

1-Chloropyrido[3,4-d]pyridazine

Ref: 54-OR450000