1. Home
  2. Phosphine,(6,6'-dimethoxy[1,1'-biphenyl]-2,2'-diyl)bis[bis(4-methylphenyl)-, (R)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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,(6,6'-dimethoxy[1,1'-biphenyl]-2,2'-diyl)bis[bis(4-methylphenyl)-, (R)-

Request for Quotation
Chemical Name: Phosphine,(6,6'-dimethoxy[1,1'-biphenyl]-2,2'-diyl)bis[bis(4-methylphenyl)-, (R)-
CAS Number: 133545-24-1
Product Number: AG003C6I(AGN-PC-0PK1BF)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
488.5g/mol
XLogP3:
8.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
6
Exact Mass:
488.182275g/mol
Monoisotopic Mass:
488.182275g/mol
Topological Polar Surface Area:
0Ų
Heavy Atom Count:
35
Formal Charge:
0
Complexity:
587
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


In chemical synthesis, (R)-(+)-2,2'-Bis(di-p-tolylphosphino)-6,6'-dimethoxy-1,1'-biphenyl serves as a versatile chiral ligand that plays a critical role in asymmetric catalysis. Due to its unique structural properties and chirality, this compound is particularly valued for its ability to differentiate between enantiomers and facilitate the formation of enantiomerically pure products. When used in transition metal-catalyzed reactions, this ligand can control the stereochemistry of the resulting compounds, allowing for the selective synthesis of chiral molecules with high enantiomeric excess. Its application in chemical synthesis extends to a wide range of reactions, including asymmetric hydrogenation, asymmetric allylic substitution, and asymmetric cycloaddition, making it an indispensable tool for organic chemists seeking to access chiral compounds efficiently and selectively.