CAS 340267-36-9
:3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-TRIFLUOROMETHYLISOXAZOLE
Description:
3-(4-Methylsulphonylphenyl)-4-phenyl-5-trifluoromethylisoxazole, identified by its CAS number 340267-36-9, is a synthetic organic compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This compound features a trifluoromethyl group, which enhances its lipophilicity and may contribute to its biological activity. The presence of a methylsulfonyl group on the phenyl ring suggests potential for increased solubility in polar solvents and may influence its reactivity and interaction with biological targets. The phenyl groups attached to the isoxazole core can provide additional stability and may play a role in the compound's pharmacological properties. Overall, this compound's unique structural features may render it of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. However, detailed studies on its biological activity, toxicity, and pharmacokinetics would be necessary to fully understand its potential applications.
Formula:C17H12F3NO3S
Synonyms:- 3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-TRIFLUOROMETHYLISOXAZOLE
- 3-(4-methylsulfonylphenyl)-4-phenyl-5-(trifluoromethyl)-1,2-oxazole
- CAY10404
- Isoxazole, 3-[4-(methylsulfonyl)phenyl]-4-phenyl-5-(trifluoromethyl)-
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Found 4 products.
3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-TRIFLUOROMETHYLISOXAZOLE
CAS:Formula:C17H12F3NO3SPurity:98%Color and Shape:SolidMolecular weight:367.34233-(4-(Methylsulfonyl)Phenyl)-4-Phenyl-5-(Trifluoromethyl)Isoxazole
CAS:3-(4-(Methylsulfonyl)Phenyl)-4-Phenyl-5-(Trifluoromethyl)IsoxazolePurity:99%Molecular weight:367.34g/molCAY10404
CAS:CAY10404: potent COX-1/2 inhibitor; blocks PKB/Akt, MAPK pathways; triggers NSC-LC apoptosis; analgesic, anti-inflammatory, anti-cancer.Formula:C17H12F3NO3SPurity:99.02%Color and Shape:SolidMolecular weight:367.34
