Dichloro(1,5-cyclooctadiene)platinum(II)
Dichloro(1,5-cyclooctadiene)platinum(II)
  • CAS No.:12080-32-9
Other grades of this product :
Dichloro(1,5-cyclooctadiene)platinum(II) Basic information
Product Name:Dichloro(1,5-cyclooctadiene)platinum(II)
Synonyms:pt(cod)cl2;Dichloro(1,5-cyclooctadiene)platinum(II) 250 dec.;Dichloro(1,5-cyclooctadiene)platinum(II),98%;Dichloro(1,5-cyclooctadiene)platinum(II), Pt 51.6-52.6%;Dichloro(1,5-cyclooctadiene)platinum(II),99%;5-cyclooctadiene)platinum(II);Dichloro(cycloocta-1,5-diene)platinum(II),Pt52.1%;Dichloro(1,5-cyclooctadiene)platinum(II) ,98% [C%:24.15-27.15%]
CAS:12080-32-9
MF:C8H12Cl2Pt
MW:374.16
EINECS:235-144-5
Product Categories:Catalysts for Organic Synthesis;Classes of Metal Compounds;Homogeneous Catalysts;Metal Complexes;Pt (Platinum) Compounds;Synthetic Organic Chemistry;Transition Metal Compounds;organometallic complexes;chemical reaction,pharm,electronic,materials;Pt
Mol File:12080-32-9.mol
Dichloro(1,5-cyclooctadiene)platinum(II) Chemical Properties
Melting point 285 °C (dec.) (lit.)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in dichloromethane
form Crystals or Crystalline Powder
color White to pale yellow
Water Solubility insoluble
Sensitive Hygroscopic
CAS DataBase Reference12080-32-9(CAS DataBase Reference)
NIST Chemistry Reference(Cyclocta-1,5-diene)platinum(ii)chloride(12080-32-9)
EPA Substance Registry SystemPlatinum, dichloro[(1,2,5,6-.eta.)-1,5-cyclooctadiene]- (12080-32-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
TSCA Yes
HS Code 28439000
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Dichloro(1,5-cyclooctadiene)platinum(II) Usage And Synthesis
Chemical Propertieswhite to pale yellow
Usesit is used in Hydrosilyation reactions.
UsesCatalyst for:
  • Hydrogenative cyclization of allenynes
  • Stereoselective tandem hydrosilylation-Hiyama coupling reactions
  • Amino alkene cyclohydroamination
  • Hydrative cyclization reactions
  • Direct amination of allylic alcohols under mild conditions
  • Potential anticancer agent

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