CAS 1502-22-3
:Cyclohexénylcyclohexanone
- 1-(2-Oxocyclohexyl)cyclohexene
- 2-(1-cyclohexen-1-yl)-Cyclohexanone
- 2-(Cyclohex-1-en-1-yl)cyclohexan-1-one
- 2-(Cyclohex-1-enyl)cyclohexanone
- Cyclohexanone, 2-(1-cyclohexen-1-yl)-
- Cyclohexenylcyclohexanone
- NSC 518776
- CHCH
2-(1-Cyclohexenyl)cyclohexanone
CAS :Formule :C12H18ODegré de pureté :>85.0%(GC)Couleur et forme :Colorless to Light orange to Yellow clear liquidMasse moléculaire :178.282-(1-Cyclohexenyl)cyclohexanone, 85+%, cont. ca 10% 2-cyclohexylidenecyclohexanone
CAS :It is a perfuming agent. It is used for special solvents and as a raw material in agrochemicals and dyestuffs. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original
Formule :C12H18ODegré de pureté :85+%Couleur et forme :Liquid, Clear colorless to pale yellowMasse moléculaire :178.28Cyclohexanone, 2-(1-cyclohexen-1-yl)-
CAS :Formule :C12H18ODegré de pureté :98%Couleur et forme :LiquidMasse moléculaire :178.27072-(1-Cyclohexenyl)Cyclohexanone
CAS :2-(1-Cyclohexenyl)CyclohexanoneDegré de pureté :85%, cont. ca 10% 2-cyclohexylidenecyclohexanoneMasse moléculaire :178.28g/mol[1,1'-Bi(cyclohexan)]-1'-en-2-one
CAS :[1,1'-Bi(cyclohexan)]-1'-en-2-one
Degré de pureté :95%Masse moléculaire :178.28g/mol2-(1-Cyclohexenyl)cyclohexanone
CAS :2-(1-Cyclohexenyl)cyclohexanone (CCH) is a growth factor that belongs to the group of p2 class. It has been shown to inhibit the activity of thymidylate synthase, an enzyme that catalyzes the conversion of deoxyuridine 5'-triphosphate to thymidylate. CCH also inhibits cancer cell growth by inhibiting DNA synthesis and protein synthesis. The inhibition of this enzyme is thought to be due to its ability to form covalent bonds with amino groups on proteins, which prevents them from functioning as enzymes. CCH is synthesized in mitochondria and activated by hydrochloric acid, which converts it into a reactive species. This reactive species then reacts with unsaturated alkyl chains on fatty acids and reacts with aromatic hydrocarbons in the cell membrane, causing lipid peroxidation and cellular damage. The reaction mechanism for CCH involves ethylene diamine (ED) and
Formule :C12H18ODegré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :178.27 g/mol2-(1-Cyclohexenyl)cyclohexanone
CAS :Formule :C12H18ODegré de pureté :98%Couleur et forme :Liquid, No data available.Masse moléculaire :178.275





