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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, [(1S,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]diphenyl-

C[C@@H]1CC[C@H]([C@H](C1)P(c1ccccc1)c1ccccc1)C(C)C Request for Quotation
Chemical Name: Phosphine, [(1S,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]diphenyl-
CAS Number: 43077-29-8
Product Number: AG003BAX(AGN-PC-0OADW5)
Synonyms:
MDL No:
Molecular Formula: C22H29P
Molecular Weight: 324.4394

Identification/Properties

Properties
MP:
95-99 °C
BP:
414.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
air sensitive
Computed Properties
Molecular Weight:
324.448g/mol
XLogP3:
6.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
4
Exact Mass:
324.201g/mol
Monoisotopic Mass:
324.201g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
320
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
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-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chiral ligand, (1S,2S,5R)-2-Isopropyl-5-methylcyclohexyl)diphenylphosphine, plays a crucial role in chemical synthesis as a versatile tool for controlling stereochemistry in various reactions. This compound is commonly employed in asymmetric catalysis, specifically in transition metal-catalyzed processes. By coordinating with transition metals such as palladium or rhodium, this chiral ligand facilitates the formation of chiral products with high enantioselectivity. Its unique structure imparts a high degree of control over the orientation of reactants in the catalytic process, leading to the selective formation of single enantiomers. Additionally, the steric and electronic properties of this ligand contribute to its effectiveness in promoting stereoselective transformations, making it a valuable asset in organic synthesis for the production of pharmaceuticals, agrochemicals, and other fine chemicals.