4-tert-Butylacetophenone

CAS : 943-27-1

Ref. 3D-FB19505

Informations sur le produit

• Nom: 4-tert-Butylacetophenone
• Synonymes: 1-[4-(1,1-Dimethylethyl)phenyl]ethanone1-(4-tert-Butylphenyl)ethanone4-tert-Butylphenyl methyl ketone, 1-(4-Tert-Butylphenyl)Ethanone, 1-[4-(1,1-Dimethylethyl)phenyl]ethanone, 1-[4-(tert-Butyl)phenyl]ethan-1-one, 4-t-Butylacetophenone, 4-tert-Butylphenyl methyl ketone, Acetophenone, 4′-tert-butyl-, Ethanone, 1-[4-(1,1-dimethylethyl)phenyl]-, NSC 826, p-tert-Butylacetophenone, p-tert-Butylacetylbenzene, 4′-tert-Butylacetophenone

Description

4-tert-Butylacetophenone is an organic compound that is used to synthesize a variety of derivatives. It has been shown to have anticancer activity in vitro and in vivo, as well as antiviral activity against human pathogens. 4-tert-Butylacetophenone has also been shown to be active against Trichophyton mentagrophytes, a fungus that causes athlete's foot, and Cryptococcus neoformans, which is a pathogenic yeast that causes cryptococcal meningitis. The synthesis of 4-tert-butylacetophenone begins with the reaction of phosphorus pentoxide with a molecule of acetic acid in the presence of water. This reaction produces water and trichloroacetic acid as byproducts. The chloride ion then reacts with the trichloroacetic acid to form 4-tert-butylchloroacetic acid, which can then be reacted with phosphorous pentoxide again to

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 176.25 g/mol
• Formule: C₁₂H₁₆O
• Degré de pureté: Min. 95%
• Couleur/Forme: Colorless Clear Liquid
• InChI: InChI=1S/C12H16O/c1-9(13)10-5-7-11(8-6-10)12(2,3)4/h5-8H,1-4H3
• Code InChI: InChIKey=UYFJYGWNYQCHOB-UHFFFAOYSA-N
• SMILES: CC(=O)c1ccc(C(C)(C)C)cc1