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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Phosphine, 1,2-ethanediylbis[(2-methoxyphenyl)phenyl-, (1S,1'S)-

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Chemical Name: Phosphine, 1,2-ethanediylbis[(2-methoxyphenyl)phenyl-, (1S,1'S)-
CAS Number: 97858-62-3
Product Number: AG00IJZO(AGN-PC-0W7MA1)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
458.478g/mol
XLogP3:
5.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
9
Exact Mass:
458.156g/mol
Monoisotopic Mass:
458.156g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
472
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 1,2-Bis((S)-(2-methoxyphenyl)(phenyl)phosphino)ethane is commonly utilized as a chiral diphosphine ligand in various transition metal-catalyzed reactions. Due to its unique structure and stereochemistry, this compound plays a crucial role in asymmetric catalysis, allowing for the selective formation of enantiomerically pure products. It is particularly effective in promoting asymmetric hydrogenation, hydroformylation, and carbon-carbon bond forming reactions. The presence of the phosphine groups in this ligand facilitates the coordination with metal centers, enabling the control of regio- and stereochemistry in the desired chemical transformations. Overall, the use of 1,2-Bis((S)-(2-methoxyphenyl)(phenyl)phosphino)ethane in chemical synthesis enables chemists to access a wide range of chiral compounds with high levels of enantioselectivity.