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| | RUTHENIUM CARBONYL Basic information | | Reactions |
| | RUTHENIUM CARBONYL Chemical Properties |
| Hazard Codes | F,Xn | | Risk Statements | 11-20-2017/11/20 | | Safety Statements | 24/25 | | RIDADR | 1325 | | WGK Germany | 3 | | Hazard Note | Flammable/Harmful | | TSCA | Yes | | HazardClass | 6.1 | | PackingGroup | II | | HS Code | 28439000 |
| | RUTHENIUM CARBONYL Usage And Synthesis |
| Reactions |
- Catalyst for the conversion of enynes to catechol derivatives.
- Catalyst for the intermolecular [2+2+1] cycloaddition of ketones, CO and alkenes or alkynes.
- 3-Component couplings.
- Reaction of α,β-unsaturated imines with carbon monoxide and alkenes to form β,γ-unsaturated γ-butyroactams.
- Ester decarboxylation.
- Catalyst for hydroamination and C-H bond activation.
- Used in sp3 C-H bond arylation and carbonylation.
- Ru/halide catalytic system for C-C bond forming reaction between alkynes and unsaturated carbonyl compounds.
- Amination of α-hydroxy amides.
| | Chemical Properties | orange plates | | Uses | A H-transfer catalyst. It is used in carbonylation catalysis of the allylic amination of unactivated olefins by nitroarenes, reductive carbonylation of mononitro aromatic compounds to carbamates, and as a catalyst for cycloaddition reactions. It is employed as a precursor for the synthesis of Ru nanoparticles. Catalyst used in the intermolecular [3+2+1] cycloaddition of alpha,beta-unsaturated ketones with silylacetylenes and carbon monoxide, to produce alpha-pyrones. Catalyzes the coupling of silanes with thiols, alcohols and amines with high turnover number (TON) and high turnover frequency (TOF). | | General Description | Atomic number of base material: 44 Ruthenium |
| | RUTHENIUM CARBONYL Preparation Products And Raw materials |
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