CAS 67189-27-9
:2-(2,4-dichlorophenyl)-1,3-thiazolidine
Description:
2-(2,4-Dichlorophenyl)-1,3-thiazolidine is a chemical compound characterized by its thiazolidine ring structure, which incorporates a sulfur atom and a nitrogen atom within a five-membered ring. The presence of the 2,4-dichlorophenyl group indicates that the compound has two chlorine substituents on the phenyl ring, contributing to its potential biological activity and lipophilicity. This compound is typically studied for its pharmacological properties, as thiazolidines are known to exhibit various biological activities, including anti-inflammatory and antimicrobial effects. The molecular structure suggests that it may interact with biological targets due to the electron-withdrawing nature of the chlorine atoms, which can influence the compound's reactivity and solubility. Additionally, the thiazolidine framework can participate in various chemical reactions, making it a versatile building block in organic synthesis. Safety and handling precautions should be observed, as with many chemical substances, due to potential toxicity or environmental impact.
Formula:C9H9Cl2NS
InChI:InChI=1/C9H9Cl2NS/c10-6-1-2-7(8(11)5-6)9-12-3-4-13-9/h1-2,5,9,12H,3-4H2
SMILES:c1cc(c(cc1Cl)Cl)C1NCCS1
Synonyms:- Thiazolidine, 2-(2,4-Dichlorophenyl)-
- 2-(2,4-Dichlorophenyl)-1,3-thiazolidine
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