Dichlorotris(triphenylphosphine)ruthenium(II)
Product Information
Molecular Formula
RuCl2(P(C6H5)3)3
Molecular Weight
958.83
Description
Dichlorotris(triphenylphosphine)ruthenium(II) is a crucial biomedical agent employed in the management of malignancies and diverse ailments. It serves as a highly proficient catalyst within numerous organic reactions, encompassing hydrogenation, isomerization, and dehydrogenation processes. This compound exemplifies remarkable therapeutical promise owing to its potent anticancer attributes targeting lung, breast, and ovarian carcinoma cell lines. Ongoing investigations are diligently unraveling its potential employment as part of drug delivery systems and precision therapies.
Synonyms
Tris(triphenylphosphine)ruthenium(II) chloride; Dichlorotris(triphenylphosphine)ruthenium(II); Tris(triphenylphosphine)ruthenium(II) dichloride; Dichlorotris(triphenylphosphino)ruthenium (II); Ruthenium(II)-tris(triphenylphosphine) dichloride; Dichlorotris(triphenylphosphine)ruthenium; Tris(triphenylphosphine)dichlororuthenium; RuCl2(PPh3)3; Tris(triphenylphosphine)ruthenium(II)Dichloride; dichlororuthenium,triphenylphosphane; Tris(triphenylphosphine)ruthenium(II) Dichloride
IUPAC Name
dichlororutheniumtriphenylphosphane
SMILES
C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.Cl[Ru]Cl
InChI
InChI=1S/3C18H15P.2ClH.Ru/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h3*1-15H2*1H/q+2/p-2
InChI Key
WIWBLJMBLGWSIN-UHFFFAOYSA-L
Purity
>90.0%(T)
Appearance
Dark green to Dark blue to Black powder to crystal
Safety Information
Hazards
H302 + H312 + H332
Precautionary Statement
P501 P261 P270 P271 P264 P280 P362+P364 P301 + P312 + P330 P302 + P352 + P312 P304 + P340 + P312
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
9
Exact Mass
958.115458 g/mol
Monoisotopic Mass
958.115458 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
60
Formal Charge
0
Complexity
204
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
4
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| US-4321414-A | Catalytic hydrogenation of glycolaldehyde to produce ethylene glycol | 1980-08-26 |
| US-4317946-A | Process for producing ethylene glycol via catalytic hydrogenation of glycolaldehyde | 1980-06-27 |
