CAS 19982-38-8
:5-(2-ETHOXYPHENYL)-1,3,4-OXADIAZOLE-2-THIOL
Description:
5-(2-Ethoxyphenyl)-1,3,4-oxadiazole-2-thiol is a chemical compound characterized by its unique oxadiazole ring structure, which incorporates a thiol functional group. This compound features an ethoxy group attached to a phenyl ring, contributing to its potential solubility and reactivity. The oxadiazole moiety is known for its applications in various fields, including pharmaceuticals and materials science, due to its heterocyclic nature and ability to participate in diverse chemical reactions. The presence of the thiol group enhances its reactivity, allowing for potential applications in synthesis and as a ligand in coordination chemistry. Additionally, compounds like this may exhibit interesting biological activities, making them subjects of interest in medicinal chemistry. The molecular structure and functional groups present in 5-(2-ethoxyphenyl)-1,3,4-oxadiazole-2-thiol suggest that it could be explored for various applications, including as an intermediate in organic synthesis or as a potential therapeutic agent. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.
Formula:C10H10N2O2S
InChI:InChI=1/C10H10N2O2S/c1-2-13-8-6-4-3-5-7(8)9-11-12-10(15)14-9/h3-6H,2H2,1H3,(H,12,15)
SMILES:CCOc1ccccc1c1nnc(o1)S
Synonyms:- 1,3,4-Oxadiazole-2(3H)-thione, 5-(2-ethoxyphenyl)-
- 19982-38-8
- 5-(2-ethoxyphenyl)-1,3,4-oxadiazole-2(3H)-thione
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Found 2 products.
5-(2-Ethoxyphenyl)-1,3,4-oxadiazole-2-thiol
CAS:5-(2-Ethoxyphenyl)-1,3,4-oxadiazole-2-thiol is a versatile compound that has various applications in different industries. It is commonly used as a research chemical and as a catalyst in industrial processes. This compound is known for its brominated dimers and its ability to undergo sulfoxidation and n-oxide formation.Formula:C10H10N2O2SPurity:Min. 95%Molecular weight:222.27 g/mol

