CAS 5406-39-3
:(4E)-4-[4-(benzyloxy)benzylidene]-3-phenyl-1,2-oxazol-5(4H)-one
Description:
The chemical substance known as (4E)-4-[4-(benzyloxy)benzylidene]-3-phenyl-1,2-oxazol-5(4H)-one, with the CAS number 5406-39-3, is an organic compound characterized by its oxazole ring structure, which is a five-membered heterocyclic compound containing nitrogen and oxygen. This compound features a phenyl group and a benzyloxy substituent, contributing to its potential applications in organic synthesis and medicinal chemistry. The presence of the benzylidene moiety indicates that it may exhibit interesting electronic properties and reactivity, making it a candidate for further study in various chemical reactions. Its structural features suggest potential biological activity, which could be explored in pharmacological contexts. Additionally, the compound's stability and solubility characteristics would be important for its practical applications, particularly in drug formulation or as a reagent in organic synthesis. Overall, this compound represents a class of oxazole derivatives that may possess unique chemical and biological properties worthy of investigation.
Formula:C23H17NO3
InChI:InChI=1/C23H17NO3/c25-23-21(22(24-27-23)19-9-5-2-6-10-19)15-17-11-13-20(14-12-17)26-16-18-7-3-1-4-8-18/h1-15H,16H2/b21-15+
Synonyms:- 5(4H)-isoxazolone, 3-phenyl-4-[[4-(phenylmethoxy)phenyl]methylene]-, (4E)-
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Found 3 products.
3-(4-Methylphenyl)propan-1-ol
CAS:<p>3-(4-Methylphenyl)propan-1-ol is a compound that is used as an intermediate in organic synthesis. It has been shown to undergo regioselective radical cyclization reactions with cations and radical cations, yielding the corresponding methylenecyclopropane derivatives. 3-(4-Methylphenyl)propan-1-ol can be used as a precursor for various other compounds, such as ethyl (2E)-3-[4-(methylphenyl)buta-1,3-diene]propanoate.</p>Formula:C10H14OPurity:Min. 95%Molecular weight:150.22 g/mol
