Trans-N1-(3-Pyridinylmethyl)-1,4-cyclohexanediamine is a chemical compound characterized by its unique structure, which includes a cyclohexane ring substituted with two amine groups and a pyridine moiety. This compound typically exhibits properties associated with both amines and heterocycles, such as basicity due to the presence of nitrogen atoms. The trans configuration indicates that the substituents on the cyclohexane ring are positioned opposite each other, which can influence its spatial orientation and reactivity. The pyridine ring contributes to the compound's potential for forming coordination complexes and may enhance its solubility in polar solvents. Additionally, the presence of multiple functional groups suggests that it may participate in various chemical reactions, including nucleophilic substitutions and hydrogen bonding. This compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological targets. Overall, trans-N1-(3-Pyridinylmethyl)-1,4-cyclohexanediamine is a versatile compound with potential significance in both research and industrial applications.

trans-N1-(3-Pyridinylmethyl)-1,4-cyclohexanediamine

890652-01-4: Trans-N1-(3-Pyridinylmethyl)-1,4-cyclohexanediamine is a chemical compound characterized by its unique structure, which includes a cyclohexane ring substituted with two amine groups and a pyridine moiety. This compound typically exhibits properties associated with both amines and heterocycles, such as basicity due to the presence of nitrogen atoms. The trans configuration indicates that the substituents on the cyclohexane ring are positioned opposite each other, which can influence its spatial orientation and reactivity. The pyridine ring contributes to the compound's potential for forming coordination complexes and may enhance its solubility in polar solvents. Additionally, the presence of multiple functional groups suggests that it may participate in various chemical reactions, including nucleophilic substitutions and hydrogen bonding. This compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological targets. Overall, trans-N1-(3-Pyridinylmethyl)-1,4-cyclohexanediamine is a versatile compound with potential significance in both research and industrial applications.

CAS 890652-01-4

trans-N1-(3-Pyridinylmethyl)-1,4-cyclohexanediamine

1-N-(Pyridin-3-ylmethyl)cyclohexane-1,4-diamine

Ref: 3D-QKB65201