CAS 5407-98-7
:Cétones de phénylcyclobutyle
- 1-Cyclobutyl-1-phenylmethanone
- Benzoylcyclobutane
- Cyclobutane, benzoyl-
- Cyclobutyl(Phenyl)Methanone
- Cyclobutylphenylmethanone
- Ketone, cyclobutyl phenyl
- Methanone, cyclobutylphenyl-
- NSC 10744
- Phenyl cyclobutyl ketone
- Cyclobutyl phenyl ketone
Cyclobutyl Phenyl Ketone
CAS :Formule :C11H12ODegré de pureté :>95.0%(GC)Couleur et forme :Colorless to Yellow to Green clear liquidMasse moléculaire :160.22Methanone, cyclobutylphenyl-
CAS :Formule :C11H12ODegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :160.2124Cyclobutyl Phenyl Ketone
CAS :Cyclobutyl Phenyl KetoneDegré de pureté :98%Masse moléculaire :160.21g/molCyclobutyl phenyl ketone
CAS :Formule :C11H12ODegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :160.216Cyclobutyl Phenyl Ketone
CAS :Cyclobutyl Phenyl Ketone is an unsaturated ketone that belongs to the class of aliphatic hydrocarbons. It is used in vitro assays as a receptor binding agent. Cyclobutyl Phenyl Ketone can bind to the benzodiazepine site on GABA-A receptors, which are a type of neurotransmitter receptor found in the central nervous system. Cyclobutyl Phenyl Ketone has been shown to be effective in treating chronic bronchitis due to its ability to inhibit chloride ion uptake by human lung cells. This compound has also been shown to be effective for treating bladder cancer due to its function as a hydrogen chloride scavenger and nitro group donor. Cyclobutyl Phenyl Ketone can be synthesized from ethyl formate, through a Friedel-Crafts reaction with hydrogen chloride, followed by carbonyl reduction with sodium borohydride. The asymmetric synthesis of this compound requires a simple modification in the starting material,
Formule :C11H12ODegré de pureté :Min. 95%Masse moléculaire :160.22 g/mol




