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132071-87-5

Ruthenium, [(1R)-[1,1'-binaphthalene]-2,2'-diylbis[diphenylphosphine-κP]]dichloro-, (SP-4-2)- (9CI)

Catalog#: AR0010UD  |   CAS#: 132071-87-5  |   MDL#: MFCD01073794  |   MF: C44H32Cl2P2Ru  |   MW: 794.6484

Packsize Purity Price Availability Quantity
100mg 98% $6.00 Global Stock Buy Now Add To Cart
250mg 98% $7.00 Global Stock Buy Now Add To Cart
1g 98% $23.00 Global Stock Buy Now Add To Cart
5g 98% $111.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0010UD
Chemical Name Ruthenium, [(1R)-[1,1'-binaphthalene]-2,2'-diylbis[diphenylphosphine-κP]]dichloro-, (SP-4-2)- (9CI)
CAS Number 132071-87-5
Molecular Formula C44H32Cl2P2Ru
Molecular Weight 794.6484
MDL Number MFCD01073794
SMILES c1ccc(cc1)P(c1ccc2c(c1c1c(ccc3c1cccc3)P(c1ccccc1)c1ccccc1)cccc2)c1ccccc1.Cl[Ru]Cl

[2,2'-Bis(diphenylphosphino)-(R)-1,1'-binaphthyl]dichlororuthenium, also known as $name$, is a highly versatile organometallic compound widely employed in chemical synthesis applications. This complex ruthenium catalyst plays a crucial role in catalyzing various organic transformations, particularly in asymmetric synthesis.One significant application of $name$ in chemical synthesis is its utility in asymmetric hydrogenation reactions. By utilizing its chiral ligands, this ruthenium catalyst can facilitate the selective reduction of unsaturated compounds to form chiral products with high enantioselectivity. This capability is particularly valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where enantiopurity is essential.Moreover, $name$ has been instrumental in promoting a range of other synthetic transformations, including carbon-carbon bond formations, rearrangements, and cross-coupling reactions. Its high activity and selectivity make it a valuable tool for chemists seeking to access complex molecular architectures efficiently and with precise control over stereochemistry.In summary, the application of [2,2'-Bis(diphenylphosphino)-(R)-1,1'-binaphthyl]dichlororuthenium in chemical synthesis offers a powerful and effective means for conducting asymmetric transformations and accessing structurally diverse compounds with high levels of stereochemical control. Its versatility and efficiency make it a cornerstone in the toolbox of synthetic chemists striving to create novel molecules with specific chirality and functionality.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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