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

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

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
Product Categories:
  • Rh
  • organometallic complex
  • Catalysis and Inorganic Chemistry
  • Chemical Synthesis
  • Rhodium
Mol File:
99326-34-8.mol
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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 limits
ACGIH: TWA 1 mg/m3
NIOSH: IDLH 100 mg/m3; TWA 0.1 mg/m3
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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

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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

Chemical Properties

dark red crystals

Uses

Umicore Precatalysts for Asymmetric and Cross-Coupling Catalysis

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