CAS 56077-28-2
:2-Bromo-1-cyclohexyléthanone
- (Bromoacetyl)cyclohexane
- 1-Bromo-2-cyclohexylethan-2-one
- 2-Bromo-1-cyclohexylethan-1-one
- Bromomethyl cyclohexyl ketone
- Cyclohexyl bromomethyl ketone
- Ethanone, 2-Bromo-1-Cyclohexyl-
- Ethanone, 2-bromo-1-cyclohexyl-(9CI)
- Ketone, bromomethyl cyclohexyl
- 2-Bromo-1-cyclohexylethanone
2-Bromo-1-cyclohexylethanone
CAS :Formule :C8H13BrODegré de pureté :97%Couleur et forme :LiquidMasse moléculaire :205.09222-Bromo-1-cyclohexylethan-1-one
CAS :2-Bromo-1-cyclohexylethan-1-oneDegré de pureté :97%Masse moléculaire :205.095g/mol2-Bromo-1-cyclohexylethanone
CAS :Formule :C8H13BrODegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :205.0952-Bromo-1-cyclohexylethanone
CAS :Produit contrôléApplications 2-Bromo-1-cyclohexylethanone
Formule :C8H13BrOCouleur et forme :NeatMasse moléculaire :205.0922-Bromo-1-cyclohexylethanone
CAS :2-Bromo-1-cyclohexylethanone is an organic compound with a cyclohexane ring and two bromine atoms. It has been shown to be an inhibitor of the immunoproteasome, which is a protein complex that degrades proteins in the cell. This inhibition results in increased concentrations of hydrogen peroxide, which has antioxidant properties. 2-Bromo-1-cyclohexylethanone also has radical scavenging activity, which prevents the oxidation of other molecules by reactive oxygen species. This compound has shown medicinal values for autoimmune diseases, inflammatory diseases, and allergies. The flavonoids contained in 2-bromo-1-cyclohexylethanone are responsible for its antiallergic effects and its ability to inhibit histamine release from mast cells. 2-Bromo-1-cyclohexylethanone is stereoselective in inhibiting the immunoproteasome as it binds to only
Formule :C8H13BrODegré de pureté :Min. 95%Masse moléculaire :205.09 g/mol




