CHLORO(1,5-CYCLOOCTADIENE)(PENTAMETHYLCYCLOPENTADIENYL)RUTHENIUM (II)

CHLORO(1,5-CYCLOOCTADIENE)(PENTAMETHYLCYCLOPENTADIENYL)RUTHENIUM (II)
  • CAS No.:92390-26-6
Other grades of this product :
CHLORO(1,5-CYCLOOCTADIENE)(PENTAMETHYLCYCLOPENTADIENYL)RUTHENIUM (II) Basic information
Reactions
Product Name:CHLORO(1,5-CYCLOOCTADIENE)(PENTAMETHYLCYCLOPENTADIENYL)RUTHENIUM (II)
Synonyms:(1,5-cyclooctadiene) (pentamethylcyclopentadiene) rubidium chloride;Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium(II),98%;Ruthenium,chloro[(1,2,5,6-h)-1,5-cyclooctadiene][(1,2,3,4,5-h)-1,2,3,4,5-pentamethyl-2,4-cyclopentadien-1-yl]-;1,5-Cyclooctadiene, ruthenium complex;Chloro(1,5-cyclooctadiene)(η5-pentamethylcyclopentadienyl)ruthenium;Cp*RuCl(cod);Chloro(1,5-cyclooctadiene)(pentamethylcyclopent...;Chloro(pentamethylcyclopentadienyl)(cyclooctadiene)ruthenium(II)
CAS:92390-26-6
MF:C18H27ClRu5*
MW:379.93
EINECS:
Product Categories:Ru;organometallic complex
Mol File:92390-26-6.mol
CHLORO(1,5-CYCLOOCTADIENE)(PENTAMETHYLCYCLOPENTADIENYL)RUTHENIUM (II) Chemical Properties
Melting point 143-147℃
storage temp. -20°C
color brown microxtls
Stability:store cold
InChIKeyJBVMVFXUVNUNNG-ONEVTFJLSA-M
Safety Information
Hazard Codes F
Risk Statements 20/21/22-14/15
Safety Statements 22-36/37/39-43
RIDADR UN 3395
WGK Germany 3
TSCA No
HazardClass 4.3
MSDS Information
CHLORO(1,5-CYCLOOCTADIENE)(PENTAMETHYLCYCLOPENTADIENYL)RUTHENIUM (II) Usage And Synthesis
Reactions
  1. Catalyst for regio and stereo-specific ring opening via N-O bond cleavage.
  2. Catalyst for transformation of 1,6-enynes and diazoalkanes into alkenylbicyclo[3.1.0]hexane derivatives.
  3. Catalyst for ring closing enyne metathesis.
  4. Catalyst for [2 + 2 + 2] cocyclization of diene-yne, and cyclodimerization of allenynes.
  5. Catalyst for hydrovinylation of ynamides with ethylene.
  6. Catalyst for C–H insertion reactions of carbenes. 
UsesChloro(pentamethylcyclopentadienyl)(cyclooctadiene)ruthenium(II) is a homogeneous catalyst for the formation of carbon-carbon and carbon-heteroatom bonds.It can be used:
  • To catalyze cyclotrimerization of alkynylboronates, propargyl alcohols, and terminal alkynes to form arylboronate, which in turn undergoes palladium(II)-catalyzed carbonylation to form highly substituted phthalides.
  • To catalyze C-C coupling of norbornenes and norbornadiene with alkynes?to form [2 + 2] cycloadducts.
  • In combination with 2-diphenylphosphinoethylamine-potassium tertiary butoxide to form a ternary catalyst system that can catalyze fast racemization of chiral non-racemic sec-alcohols.
  • To synthesize new organoruthenium complexes with phosphorus-based ligands such as bis(phosphino)amines.
  • To catalyze the addition of organic disulfides to alkenes leading to vic-dithioethers.
CHLORO(1,5-CYCLOOCTADIENE)(PENTAMETHYLCYCLOPENTADIENYL)RUTHENIUM (II) Preparation Products And Raw materials

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