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Home  > Dibenzo[d,f][1,3,2]dioxaphosphepin, 6,6'-[[3,3'-bis(1,1-dimethylethyl)-5,5'-dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis(oxy)]bis-

AA53506

121627-17-6 | Dibenzo[d,f][1,3,2]dioxaphosphepin, 6,6'-[[3,3'-bis(1,1-dimethylethyl)-5,5'-dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis(oxy)]bis-

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $32.00 $23.00 -   +
1g 97% in stock $236.00 $165.00 -   +

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Description
Catalog Number: AA53506
Chemical Name: Dibenzo[d,f][1,3,2]dioxaphosphepin, 6,6'-[[3,3'-bis(1,1-dimethylethyl)-5,5'-dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis(oxy)]bis-
CAS Number: 121627-17-6
Molecular Formula: C46H44O8P2
Molecular Weight: 786.7843
MDL Number: MFCD00233876
SMILES: COc1cc(c(c(c1)c1cc(OC)cc(c1Op1oc2ccccc2c2c(o1)cccc2)C(C)(C)C)Op1oc2ccccc2c2c(o1)cccc2)C(C)(C)C

 

Upstream Synthesis Route
  • 6,6'-((3,3'-Di-tert-butyl-5,5'-dimethoxy-[1,1'-biphenyl]-2,2'-diyl)bis(oxy))didibenzo[d,f][1,3,2]dioxaphosphepine is a versatile compound widely utilized in chemical synthesis as a highly efficient and selective phosphine ligand. When employed in transition metal catalyzed reactions, this molecule exhibits exceptional coordination capabilities, allowing for intricate control over reaction pathways and facilitating the formation of desired products with high yields and purity. Its unique structural features, including the presence of tert-butyl and dimethoxy groups on the biphenyl backbone, contribute to its steric and electronic properties, enabling tailored interactions with metal centers and substrates. In various organic transformations such as cross-coupling reactions, hydrogenation, and asymmetric catalysis, this ligand plays a crucial role in promoting key bond-forming processes and enhancing overall reaction efficiency. Its application in chemical synthesis highlights the significance of ligand design and the impact of molecular structure on catalytic outcomes.
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