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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,1,1'-[(1R)-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-indene]-7,7'-diyl]bis[1,1-bis(3,5-dimethylphenyl)-

Cc1cc(C)cc(c1)P(c1cccc2c1C1(CC2)CCc2c1c(ccc2)P(c1cc(C)cc(c1)C)c1cc(C)cc(c1)C)c1cc(C)cc(c1)C Request for Quotation
Chemical Name: Phosphine,1,1'-[(1R)-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-indene]-7,7'-diyl]bis[1,1-bis(3,5-dimethylphenyl)-
CAS Number: 917377-75-4
Product Number: AG003CC7(AGN-PC-0VV72P)
Synonyms:
MDL No:
Molecular Formula: C49H50P2
Molecular Weight: 700.8688

Identification/Properties

Properties
MP:
>300℃
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
700.887g/mol
XLogP3:
13.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
6
Exact Mass:
700.339g/mol
Monoisotopic Mass:
700.339g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
51
Formal Charge:
0
Complexity:
967
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

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Chemical Structure


The chiral compound (R)-Xyl-SDP plays a key role in chemical synthesis as a highly effective chiral ligand. Its unique molecular structure allows for precise control over stereochemistry in various transformations, making it a versatile tool for asymmetric catalysis. When used in asymmetric hydrogenation and other synthetic reactions, (R)-Xyl-SDP facilitates the production of enantiomerically pure compounds with high efficiency and selectivity. This chiral ligand has found wide application in the pharmaceutical, agrochemical, and materials science industries, enabling the synthesis of complex molecules with tailored chirality for advanced applications. By harnessing the power of (R)-Xyl-SDP, chemists can achieve greater control and precision in their synthesis strategies, paving the way for innovative discoveries and advancements in the field of organic chemistry.