CAS 6582-42-9
:1-(3,4-Dichlorophényl)-1-propanone
- 1-(3,4-Dichlorophenyl)-1-propanone
- 1-(3,4-Dichlorophenyl)propan-1-one
- 1-(3,4-Dichlorphenyl)propan-1-on
- 1-Propanone, 1-(3,4-Dichlorophenyl)-
- 229-511-9
- 3′,4′-Dichloropropiophenone
- Propiophenone, 3′,4′-dichloro-
3',4'-Dichloropropiophenone, 98%
CAS :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 Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C9H8Cl2ODegré de pureté :98%Couleur et forme :White to pale cream, Crystals or crystalline powder or fused solidMasse moléculaire :203.061-(3,4-Dichlorophenyl)propan-1-one
CAS :Formule :C9H8Cl2ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :203.06523',4'-Dichloropropiophenone
CAS :3',4'-DichloropropiophenoneFormule :C9H8Cl2ODegré de pureté :≥95%Couleur et forme :SolidMasse moléculaire :203.07g/mol3',4'-Dichloropropiophenone
CAS :Formule :C9H8Cl2ODegré de pureté :>98.0%(GC)Couleur et forme :White or Colorless to Yellow to Orange powder to lump to clear liquidMasse moléculaire :203.061-(3,4-Dichlorophenyl)propan-1-one
CAS :Formule :C9H8Cl2ODegré de pureté :98%Masse moléculaire :203.063’,4’-Dichloropropiophenone
CAS :Produit contrôléApplications 3’,4’-Dichloropropiophenone is used as a reagent in the preparation of antidepressant aryl-alkyl-piperidine derivatives. Also used in the synthesis of mGlu5 receptor negative allosteric modulators. Also in the genetic screening of compounds countering the growth of methylthioadenosine phosphorylase involved in cancer spread.
References Zheng, Y. et al.: Eur. J. Med. Chem., 54, 123 (2012); Kadariya, Y. et al.: J. Biomol. Scroon., 16, 44 (2011);Formule :C9H8Cl2OCouleur et forme :NeatMasse moléculaire :203.0653,4-Dichloropropiophenone
CAS :3,4-Dichloropropiophenone is an organic solvent that contains a chlorine atom. 3,4-Dichloropropiophenone exhibits significant activity for the removal of chlorinated phenols and other halogenated organic compounds from wastewater. The reaction mechanism of this process involves the conversion of 3,4-dichloropropiophenone to a tetranuclear thiolate complex which then reacts with the halogenated compound to form an imine. This imine is hydrolyzed by hydroxide ion to produce a chlorine-containing product and ammonia. 3,4-Dichloropropiophenone has also been shown to have antimalarial activity.Formule :C9H8Cl2ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :203.06 g/mol






