CAS 163719-73-1
:ETHYL 3-TERT-BUTYL-1,2,4-OXADIAZOLE-5-CARBOXYLATE
Description:
Ethyl 3-tert-butyl-1,2,4-oxadiazole-5-carboxylate is a chemical compound characterized by its oxadiazole ring, which contributes to its unique properties. This compound features a tert-butyl group that enhances its lipophilicity, making it more soluble in organic solvents. The ethyl ester functional group provides reactivity that can be exploited in various chemical reactions, such as esterification or nucleophilic substitution. The presence of the oxadiazole moiety imparts potential biological activity, as oxadiazoles are known for their applications in pharmaceuticals and agrochemicals. Additionally, the compound's structure suggests it may exhibit interesting electronic properties due to the conjugation within the ring system. Its CAS number, 163719-73-1, allows for easy identification in chemical databases. Overall, this compound's unique structural features and functional groups make it a subject of interest in synthetic chemistry and material science.
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Found 4 products.
1,2,4-Oxadiazole-5-carboxylic acid, 3-(1,1-dimethylethyl)-, ethyl ester
CAS:Formula:C9H14N2O3Purity:96%Color and Shape:LiquidMolecular weight:198.2191Ethyl 3-(tert-butyl)-1,2,4-oxadiazole-5-carboxylate
CAS:Ethyl 3-(tert-butyl)-1,2,4-oxadiazole-5-carboxylatePurity:96%Molecular weight:198.222g/molEthyl 3-tert-butyl-1,2,4-oxadiazole-5-carboxylate
CAS:Formula:C9H14N2O3Purity:95%Color and Shape:LiquidMolecular weight:198.222Ethyl 3-(tert-butyl)-1,2,4-oxadiazole-5-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H14N2O3Purity:Min. 95%Molecular weight:198.22 g/mol



