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Chloro(1-phenylindenyl)bis(triphenylphosphine)ruthenium(II), min. 98%

Catalog Number
ACM1360949978
Product Name
Chloro(1-phenylindenyl)bis(triphenylphosphine)ruthenium(II), min. 98%
Structure
Chloro(1-phenylindenyl)bis(triphenylphosphine)ruthenium(II), min. 98%
CAS
1360949-97-8
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Synonyms
MFCD23704804;Chloro(3-phenylindenyl)bis(triphenylphosphine)ruthenium(II);1360949-97-8;
IUPAC Name
chlororuthenium;1-phenylindene;triphenylphosphane;
Molecular Weight
852.357g/mol
Molecular Formula
C51H41ClP2Ru;
Canonical SMILES
C1=CC=C(C=C1)[C]2[CH][CH][C]3[C]2[CH][CH][CH][CH]3.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];
InChI
InChI=1S/2C18H15P.C15H11.ClH.Ru/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)15;;/h2*1-15H;1-11H;1H;/q;;;;+1/p-1;
InChI Key
GXBLCXGMSHOUEG-UHFFFAOYSA-M;
Complexity
406
Covalently-Bonded Unit Count
4
Exact Mass
852.142g/mol
Heavy Atom Count
55
Monoisotopic Mass
852.142g/mol
Rotatable Bond Count
7
Topological Polar Surface Area
0A^2
Application
Efficient, ruthenium-catalyzed S-S, S-Si, and S-B bond forming reactions.

Chemoselective oxidation of secondary alcohols to ketones.

Ruthenium complex used as an efficient transfer hydrogenation catalyst.

Catalyst for the racemization of chiral alcohols.
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