RUTHENIUM CARBONYL CAS#: 15243-33-1; ChemWhat Code: 34026
Identification
| Product Name | RUTHENIUM CARBONYL |
| Molecular Structure |  |
| CAS Registry Number | 15243-33-1 |
| MDL Number | MFCD00011209 |
| Molecular Formula | C5H6N2 |
| Molecular Weight | 94.116 |
Physical Data
| Solubility | It is soluble in water as well as soluble in alcohol, benzene. |
| Melting Point, °C |
| 144 – 145 |
| 154 – 155 |
| 154 – 156 |
| Density, g·cm-3 | Measurement Temperature, °C |
| 2.56 | -173.16 |
| 2.552 | -173.16 |
| 2.552 | -153.16 |
| 2.486 |
Spectra
| Description (NMR Spectroscopy) | Nucleus (NMR Spectroscopy) | Solvents (NMR Spectroscopy) | Temperature (NMR Spectroscopy), °C | Frequency (NMR Spectroscopy), MHz |
| Spectrum | 13C | |||
| Chemical shifts, Spectrum | 13C | benzene-d6 | 100.6 | |
| Spectrum, Linewidth of NMR absorption | other | neat (no solvent, solid phase) | ||
| other | tetrahydrofuran | 39.84 | ||
| Spectrum | 13C | not given |
| Description (IR Spectroscopy) | Solvent (IR Spectroscopy) |
| Intensity of IR bands, Bands, Spectrum | potassium bromide |
| Bands | n-heptane |
| Bands | hexane |
| Description (UV/VIS Spectroscopy) | Solvent (UV/VIS Spectroscopy) |
| Reflection spectrum, Spectrum | |
| Spectrum | |
| Band assignment, Spectrum | ethyl acetate |
| Spectrum | dichloromethane |
Route of Synthesis (ROS)
| Conditions | Yield |
| With triethylamine In propan-1-ol; water at 85℃; under 2625.26 Torr; Concentration; Reagent/catalyst; Solvent; Temperature; Pressure; Autoclave; | 92.5% |
| In methanol at 125℃; under 48754.9 Torr; for 8h; Autoclave; |
Safety and Hazards
No data available
Other Data
No data available
| Druglikeness | |
| Lipinski rules component | |
| Molecular Weight | 639.335 |
| logP | |
| HBA | 12 |
| HBD | 0 |
| Matching Lipinski Rules | 1 |
| Veber rules component | |
| Polar Surface Area (PSA) | 0 |
| Rotatable Bond (RotB) | 0 |
| Matching Veber Rules | 2 |
| Use Pattern |
| RUTHENIUM CARBONYL CAS#: 15243-33-1 is often used as a catalyst in organic synthesis. It facilitates the reaction between carbon monoxide and organic compounds, leading to the production of carbonyl compounds. These reactions are significant in the synthesis of pharmaceuticals and other organic compounds. And RUTHENIUM CARBONYL can also be employed as a catalyst in hydrogen transfer reactions, participating in reactions that enable the effective transfer of hydrogen in organic synthesis. |
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