CAS 453-69-0
:3-(4-fluorobenzyl)-2-thioxo-1,3-thiazolidin-4-one
Description:
3-(4-Fluorobenzyl)-2-thioxo-1,3-thiazolidin-4-one is a heterocyclic compound characterized by its thiazolidinone structure, which features a thiazolidine ring containing sulfur and nitrogen atoms. The presence of a thioxo group (C=S) contributes to its reactivity and potential biological activity. The 4-fluorobenzyl substituent enhances its lipophilicity and may influence its interaction with biological targets. This compound is typically studied for its potential pharmacological properties, including antimicrobial and anti-inflammatory activities. Its molecular structure allows for various chemical modifications, which can lead to derivatives with enhanced efficacy or selectivity. The compound is generally stable under standard laboratory conditions but should be handled with care due to the presence of sulfur and nitrogen, which can participate in various chemical reactions. As with many thiazolidinones, it may exhibit tautomerism, leading to different forms that could have distinct properties. Overall, 3-(4-fluorobenzyl)-2-thioxo-1,3-thiazolidin-4-one represents a class of compounds with significant interest in medicinal chemistry and drug development.
Formula:C10H8FNOS2
InChI:InChI=1/C10H8FNOS2/c11-8-3-1-7(2-4-8)5-12-9(13)6-15-10(12)14/h1-4H,5-6H2
SMILES:c1cc(ccc1CN1C(=O)CSC1=S)F
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Found 1 products.
3-[(4-Fluorophenyl)methyl]-2-sulfanylidene-1,3-thiazolidin-4-one
CAS:<p>3-[(4-Fluorophenyl)methyl]-2-sulfanylidene-1,3-thiazolidin-4-one is an inhibitor of ion channels. It binds to the alpha subunit of voltage gated potassium channels (Kv1.1) and inhibits potassium ion conductance. 3-[(4-Fluorophenyl)methyl]-2-sulfanylidene-1,3-thiazolidin-4-one has been shown to inhibit the binding of peptides and antibodies to receptors. This compound is used as a research tool for cell biology and in studies related to receptor interactions, ion channels, and peptides.</p>Formula:C10H8FNOS2Purity:Min. 95%Molecular weight:241.3 g/mol
