2-(Nitromethylene)thiazolidine is a heterocyclic organic compound characterized by the presence of a thiazolidine ring, which is a five-membered ring containing both sulfur and nitrogen atoms. The nitromethylene group (-C(NO2)=CH2) is attached to the thiazolidine structure, contributing to its reactivity and potential applications in organic synthesis. This compound typically exhibits properties such as being a solid at room temperature, with a specific melting point and solubility characteristics that depend on the solvent used. The presence of the nitro group often imparts polar characteristics, influencing its interactions with other chemical species. Additionally, 2-(Nitromethylene)thiazolidine may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its synthesis usually involves the reaction of thiazolidine derivatives with nitroalkenes or related compounds. As with many nitro-containing compounds, it is essential to handle this substance with care due to potential toxicity and reactivity.

2-(Nitromethylene)thiazolidine

66357-40-2: 2-Nitromethylenethiazolidine, (2E)-2-(nitromethylidene)-1,3-thiazolidine

2-(Nitro methylene) thiazolidine is an active methylene compound that is used as a medicine. It is catalysed by amines to form nitrosamines and reacts with xylene to form nitro compounds. 2-(Nitro methylene) thiazolidine has been shown to be synthesised in the presence of various functional groups, such as alcohols, carboxylic acids, phenols and sulfonic acids. This compound has been shown to have anticancer activity against cancer cells and aldehydes.

CAS 66357-40-2: 2-(Nitromethylene)thiazolidine

2-(Nitro methylene) thiazolidine

Ref: 3D-FN30739

Ranitidine Impurity 20

Ref: 4Z-R-0334