Phosphine,[(1S)-6,6'-dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis[bis[3,5-bis(1,1-dimethylethyl)phenyl]-


Chemical Name: Phosphine,[(1S)-6,6'-dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis[bis[3,5-bis(1,1-dimethylethyl)phenyl]-
CAS Number: 167709-31-1
Product Number: AG001XJZ(AGN-PC-0Q93K3)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties


Properties
BP:
856.5±65.0 °C(Predicted)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
1031.484g/mol
XLogP3:
22.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
17
Exact Mass:
1030.689g/mol
Monoisotopic Mass:
1030.689g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
74
Formal Charge:
0
Complexity:
1430
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:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The (S)-(-)-2,2'-Bis[di(3,5-di-t-butylphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl, commonly referred to as $name$, is a versatile chiral ligand widely employed in chemical synthesis. This compound plays a crucial role in asymmetric catalysis, where it acts as a catalyst in various reactions to induce chirality in the products.In the realm of chemical synthesis, $name$ serves as a key tool for achieving enantioselectivity in a range of transformations. Its unique structural features enable it to effectively coordinate with transition metal centers, facilitating the selective formation of chiral molecules. By harnessing the chirality of $name$, chemists can control the stereochemistry of their target compounds, leading to the production of optically pure substances with high levels of enantiomeric excess.Moreover, the exceptional performance of (S)-(-)-2,2'-Bis[di(3,5-di-t-butylphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl in catalytic processes has made it a valuable asset in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its applications extend to various organic transformations, such as asymmetric hydrogenation, cross-coupling reactions, and cycloadditions, where precise control over chiral induction is paramount.Overall, $name$ stands as a cornerstone in the field of chemical synthesis, empowering chemists to unlock new possibilities in the development of complex molecular structures with high levels of stereochemical control.