Chloro(1,5-cyclooctadiene)rhodium(I) dimer

98%

  • Product Code: 64445
  Alias:    (1,5-cyclooctadiene) rhodium chloride (I) dimer; chloride (1,5-cyclooctadiene) rhodium dimerization, dimer chloride (1,5-cyclooctadiene) rhodium ( I)
  CAS:    12092-47-6
Molecular Weight: 493.08 g./mol Molecular Formula: C₁₆H₂₄Cl₂Rh₂
EC Number: 235-157-6 MDL Number: MFCD00012415
Melting Point: 216.3-219.2 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used as a catalyst in organic synthesis, particularly in hydrogenation and hydroformylation reactions. It facilitates the addition of hydrogen to unsaturated compounds, making it valuable in the production of fine chemicals and pharmaceuticals. Also employed in the synthesis of complex organic molecules, aiding in the formation of carbon-carbon and carbon-heteroatom bonds. Its effectiveness in asymmetric synthesis is notable, enabling the production of chiral compounds with high enantioselectivity. Commonly applied in research and industrial processes for its stability and efficiency under mild reaction conditions.
Product Specification:
Test Specification
ASSAY 97.5-100
BULLION ASSAYRH 40.5-41.8
Appearance Orange Yellow-Orange or Orange-Brown?Powder, Crystals or Crystalline Powder
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $593.86
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0.500 10-20 days $1,079.75
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2.000 10-20 days $4,152.48
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Chloro(1,5-cyclooctadiene)rhodium(I) dimer
Used as a catalyst in organic synthesis, particularly in hydrogenation and hydroformylation reactions. It facilitates the addition of hydrogen to unsaturated compounds, making it valuable in the production of fine chemicals and pharmaceuticals. Also employed in the synthesis of complex organic molecules, aiding in the formation of carbon-carbon and carbon-heteroatom bonds. Its effectiveness in asymmetric synthesis is notable, enabling the production of chiral compounds with high enantioselectivity. Commonly applied in research and industrial processes for its stability and efficiency under mild reaction conditions.
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