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Home  > Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II)

AB56198

106681-15-6 | Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II)

Packsize Purity Availability Price Discounted Price    Quantity
200mg in stock $44.00 $31.00 -   +
5g in stock $620.00 $434.00 -   +

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Description
Catalog Number: AB56198
Chemical Name: Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II)
CAS Number: 106681-15-6
Molecular Formula: C52H48O4P2Ru
Molecular Weight: 899.9526
MDL Number: MFCD09753021
SMILES: Cc1ccc(cc1)P1(c2ccc(cc2)C)c2ccc3c(c2-c2c(P([Ru+2]451([O-]C(=[O]5)C)[O-]C(=[O]4)C)(c1ccc(cc1)C)c1ccc(cc1)C)ccc1c2cccc1)cccc3

 

Upstream Synthesis Route
  • Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) is a versatile organometallic compound that finds extensive application in chemical synthesis processes. This compound serves as a highly efficient catalyst in various organic transformations due to its unique structural properties and reactivity.In the field of chemical synthesis, Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) is commonly used in asymmetric catalysis. Its chiral ligand framework enables the catalysis of numerous reactions with high enantioselectivity, making it a valuable tool for the production of optically pure compounds. This catalyst is particularly effective in promoting C-C bond formations, hydrogenations, and other key transformations in organic synthesis.Moreover, Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) has shown excellent stability and recyclability, further enhancing its utility in chemical synthesis. Researchers and chemists rely on this compound to streamline complex reactions, reduce waste, and improve overall productivity in the laboratory.Through its exceptional catalytic properties and compatibility with a wide range of substrates, Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) continues to play a pivotal role in advancing the field of chemical synthesis, empowering scientists to access new pathways for the efficient preparation of valuable molecules.
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