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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)-

Pyrrolidine, 3,4-bis(diphenylphosphino)-1-(phenylmethyl)-, (3R,4R)-

c1ccc(cc1)CN1C[C@H]([C@@H](C1)P(c1ccccc1)c1ccccc1)P(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: Pyrrolidine, 3,4-bis(diphenylphosphino)-1-(phenylmethyl)-, (3R,4R)-
CAS Number: 99135-95-2
Product Number: AG003BT6(AGN-PC-0OP29K)
Synonyms:
MDL No:
Molecular Formula: C35H33NP2
Molecular Weight: 529.590742

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
529.604g/mol
XLogP3:
7.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
8
Exact Mass:
529.209g/mol
Monoisotopic Mass:
529.209g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
38
Formal Charge:
0
Complexity:
583
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3R,4R)-1-Benzyl-3,4-bis(diphenylphosphino)pyrrolidine is a highly versatile and effective chiral ligand commonly used in chemical synthesis. Due to its unique structure and properties, this compound plays a crucial role in asymmetric catalysis, particularly in metal-catalyzed reactions.In organic synthesis, this chiral ligand is often employed in transition metal-catalyzed asymmetric transformations, such as asymmetric hydrogenation, asymmetric allylation, and asymmetric alkylation reactions. Its presence can influence the stereochemistry of the reaction, resulting in the formation of enantiomerically enriched products with high optical purity.Additionally, (3R,4R)-1-Benzyl-3,4-bis(diphenylphosphino)pyrrolidine has demonstrated exceptional efficiency in promoting various types of C-C and C-N bond-forming reactions, making it an indispensable tool for the synthesis of complex organic molecules with high levels of stereocontrol.Overall, the application of this chiral ligand in chemical synthesis allows for the rapid and selective formation of chiral compounds, facilitating the development of new pharmaceuticals, agrochemicals, and materials with improved biological activity and properties.