Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate

Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate Basic information
Reaction
Product Name:Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate
Synonyms:Bis(1,5-cyclooctadiene)rhodium(I)trifluoromethanesulphonate99%;Bis-(1,5-cyclooctadiene)-rhodium trifluoromethanesulfonate;BIS(1,5-CYCLOOCTADIENE)RHODIUM(I)TRIFLUOROMETHANESULFONATE;BIS(1,5-CYCLOOCTADIENE)-TRIFLUOROMETHANESULFITORHODIUM (I);BIS(1,5-CYCLOOCTADIENE)RHODIUM(I) TRIFL&;Bis(1,5-cyclooctadiene)rhodium(I)trifluoromethanesulfonate,99%;Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethane sulphonate 99%;Bis(1,5-cyclooctadiene)rhodiuM(I) trifluoroMethanesulfonate 98%
CAS:99326-34-8
MF:C17H24F3O3RhS
MW:468.34
EINECS:
Product Categories:Rh;organometallic complex;Catalysis and Inorganic Chemistry;Chemical Synthesis;Rhodium
Mol File:99326-34-8.mol
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate Structure
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate Chemical Properties
Melting point 159 °C (dec.)(lit.)
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in chloroform
form crystal
color dark red
Water Solubility insoluble
Sensitive Air Sensitive
Exposure limitsACGIH: TWA 1 mg/m3
NIOSH: IDLH 100 mg/m3; TWA 0.1 mg/m3
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
Hazard Note Irritant
TSCA No
HS Code 28439000
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate Usage And Synthesis
Reaction
  1. Rhodium catalyzed contrasteric regiocontrolled hydrogenative couplings of nonsymmetric 1,3-diynes to ethyl glyoxalate
  2. Rhodium catalyzed reductive Mannich coupling of vinyl ketones to N-Sulfonylimines mediated by hydrogen
  3. Rhodium catalyzed asymmetric synthesis of Sitagliptin
  4. Rhodium catalyzed asymmetric hydrogenation of tetrasubstituted α,β-unsaturated ketones
Reactions of 99326-34-8_1
Reactions of 99326-34-8_2
Chemical Propertiesdark red crystals
UsesUmicore Precatalysts for Asymmetric and Cross-Coupling Catalysis
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate Preparation Products And Raw materials
Bis[1,2-bis(diphenylphosphino)ethane]palladium(0) Chloro(1,5-cyclooctadiene)iridium(I) dimer BIS(1,5-CYCLOOCTADIENE)IRIDIUM (I) TETRAFLUOROBORATE Bis(1,5-cyclooctadiene)bis(μ-diphenylphosphido)dirhodium BIS(1 5-CYCLOOCTADIENE)RHODIUM(I) Bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate 1,3-CYCLOOCTADIENE Levofloxacin Methylate Trifluoromethanesulfonic anhydride Pefloxacin mesylate Trifluoromethanesulfonic acid Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate Trifluoromethane 1,5-Cyclooctadiene Danofloxacin mesylate Rhodium

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