The chemical substance known as [4-(thiomorpholinomethyl)phenyl]-[4-(trifluoromethyl)phenyl]methanone, with the CAS number 898783-00-1, is characterized by its complex molecular structure, which includes a phenyl ring substituted with a thiomorpholinomethyl group and another phenyl ring bearing a trifluoromethyl group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential lipophilicity due to the presence of the trifluoromethyl group, which can enhance its biological activity and solubility in organic solvents. The thiomorpholine moiety may contribute to its pharmacological properties, potentially influencing interactions with biological targets. Additionally, the presence of the carbonyl group in the methanone structure suggests reactivity typical of ketones, which can participate in various chemical reactions, including nucleophilic additions. Overall, this compound may be of interest in medicinal chemistry and drug development, particularly for its potential applications in targeting specific biological pathways or as a lead compound for further modifications.

[4-(thiomorpholinomethyl)phenyl]-[4-(trifluoromethyl)phenyl]methanone

898783-00-1: The chemical substance known as [4-(thiomorpholinomethyl)phenyl]-[4-(trifluoromethyl)phenyl]methanone, with the CAS number 898783-00-1, is characterized by its complex molecular structure, which includes a phenyl ring substituted with a thiomorpholinomethyl group and another phenyl ring bearing a trifluoromethyl group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential lipophilicity due to the presence of the trifluoromethyl group, which can enhance its biological activity and solubility in organic solvents. The thiomorpholine moiety may contribute to its pharmacological properties, potentially influencing interactions with biological targets. Additionally, the presence of the carbonyl group in the methanone structure suggests reactivity typical of ketones, which can participate in various chemical reactions, including nucleophilic additions. Overall, this compound may be of interest in medicinal chemistry and drug development, particularly for its potential applications in targeting specific biological pathways or as a lead compound for further modifications.

CAS 898783-00-1

[4-(thiomorpholinomethyl)phenyl]-[4-(trifluoromethyl)phenyl]methanone

4-thiomorpholinomethyl-4′-trifluoromethylbenzophenone

Ref: 10-F204518