CAS 7733-96-2
:Methanone, (2-oxido-1,2,5-oxadiazole-3,4-diyl)bis[2-thienyl-
Description:
Methanone, (2-oxido-1,2,5-oxadiazole-3,4-diyl)bis[2-thienyl-] is a chemical compound characterized by its unique structure that includes a methanone functional group and a 1,2,5-oxadiazole ring. The presence of the thienyl groups indicates that it contains sulfur in its aromatic system, contributing to its potential reactivity and electronic properties. This compound may exhibit interesting properties such as fluorescence or photochemical activity due to its conjugated system. The oxadiazole moiety is known for its stability and can participate in various chemical reactions, making it useful in synthetic applications. Additionally, the compound may have applications in materials science, particularly in organic electronics or as a precursor for other chemical syntheses. Its CAS number, 7733-96-2, allows for easy identification in chemical databases. However, specific physical properties such as melting point, boiling point, and solubility would need to be referenced from experimental data or literature for detailed applications and handling guidelines.
Formula:C12H6N2O4S2
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Found 4 products.
3,4-Bis(2-thienylcarbonyl)-1,2,5-oxadiazol-2-ium-2-olate
CAS:<p>3,4-Bis(2-thienylcarbonyl)-1,2,5-oxadiazol-2-ium-2-olate</p>Purity:≥95%Molecular weight:306.32g/molHC-056456
CAS:<p>HC-056456 (3,4-Bis(2-thienoyl)-1,2,5-oxadiazole-N-oxide) is a CatSper channel modulator.</p>Formula:C12H6N2O4S2Purity:99.62% - 99.65%Color and Shape:SolidMolecular weight:306.32HC-056456
CAS:<p>HC-056456 is a small molecule that binds to the adenylyl cyclase and activates it. It has been shown to reversibly activate the enzyme in both an asymmetric and symmetric form, with a preference for the asymmetric form. HC-056456 has been shown to increase intracellular calcium levels by activating the adenylyl cyclase and can be used in experiments involving the study of atypical capacitation.</p>Formula:C12H6N2O4S2Purity:Min. 95%Molecular weight:306.32 g/mol


