Name | Di-mu-chlorobis(p-cymene)chlororuthenium(II) |
Synonyms | Dichloro(p-cymene)ruthenium dimer Dichloro(p-cymene)ruthenium(II) dimer DichlorobispcymenechlororutheniumIImin Tetrachlorobis(mu-4-cymene)diruthenium(II) Bis(p-cymene)diruthenium(II) tetrachloride Di--chlorobis[(p-cymene)chlororuthenium(II)] Di-mu-chlorobis(p-cymene)chlororuthenium(II) Di-μ-chlorobis[(p-cymene)chlororuthenium(II)] Di-mu-chlorobis[(p-cymene)chlororuthenium(II)] 1-methyl-4-(1-methylethyl)-, ruthenium complex Di-u-chlorobis[(p-cymene)chloro Ruthenium(II)] (p-Cymene)ruthenium(II) chloride dimer Benzene Di-micron-chlorobis(p-cymene)chlororuthenium(II) |
CAS | 52462-29-0 |
EINECS | 435-530-5 |
InChI | InChI=1/2C10H14.4ClH.2Ru/c2*1-8(2)10-6-4-9(3)5-7-10;;;;;;/h2*4-8H,1-3H3;4*1H;;/q;;;;;;2*+2/p-4 |
InChIKey | HDIYUTHATPCURB-UHFFFAOYSA-L |
Molecular Formula | C20H28Cl4Ru2 |
Molar Mass | 612.39 |
Melting Point | 247.0-250.0°C (dec.)(lit.) |
Water Solubility | insoluble |
Solubility | Chloroform (Sparingly), Ethyl Acetate (Sparingly) |
Appearance | Red orange powder |
Color | brown |
Storage Condition | Sealed in dry,Room Temperature |
Sensitive | Sensitive to light |
MDL | MFCD00064793 |
Use | Hydrosilylation Catalysts Umicore Precatalysts for Asymmetric and Cross-Coupling Catalysis Cyclometalated ruthenium complexes with arylimines and nitrogen-containing heterocycles via C- H bond activation |
Hazard Symbols | Xn - Harmful |
Risk Codes | R22 - Harmful if swallowed R36 - Irritating to the eyes R52/53 - Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. |
WGK Germany | 2 |
TSCA | No |
HS Code | 28439000 |
Introduction | Dichlorobis (4-methylisopropylphenyl) ruthenium is a catalyst that can be used in organic chemical reactions and can also be used to prepare new ruthenium (II) complexes. |
Uses | Hydrosilylation catalyst Cyclometallated ruthenium and arylimine and nitrogen-containing heterocyclic rings undergo complexation reaction through C- H bond activation. Through the reduction reaction of imine and PMHS or by hydrogen reaction, an environmentally friendly amine synthesis method is catalyzed. A practical and benign primary amine synthesis method using ruthenium to catalyze the reduction of nitriles. The N-alkylation reaction of amine and sulfonamide catalyzed by ruthenium by hydrogen reaction method. The reduction reaction of imine and PMHS or hydrogen loan reaction are used for greener amine synthesis catalyst; A mild and practical primary amine synthesis reaction catalyzed by ruthenium for nitrile reduction reaction; N-alkylation reaction catalyzed by ruthenium for amines and sulfonamines through hydrogen loan method; ruthenium ring metallization complex with arylimine and nitrogen-containing heterocycles activated by C- H bonds |