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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)-

Di(1-adamantyl)-1-piperidinylphenylphosphine

C1CCN(CC1)c1ccccc1P(C12CC3CC(C2)CC(C1)C3)C12CC3CC(C2)CC(C1)C3 Request for Quotation
Chemical Name: Di(1-adamantyl)-1-piperidinylphenylphosphine
CAS Number: 1237588-13-4
Product Number: AG000L1E(AGN-PC-0WAFYY)
Synonyms:
MDL No:
Molecular Formula: C31H44NP
Molecular Weight: 461.6615

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2-(Di(adamantan-1-yl)phosphino)phenyl)piperidine is a versatile compound commonly used in chemical synthesis as a ligand in metal-catalyzed reactions. This unique molecule's structure features the combination of a piperidine ring with a diadamantylphosphino substituent attached to a phenyl group. In catalytic processes, this compound plays a crucial role in facilitating various transformations due to its ability to coordinate with transition metals effectively.The presence of the phosphino group provides a strong coordinating ability, allowing the ligand to form stable complexes with metal centers. This coordination is instrumental in promoting catalytic reactions by enabling the activation of substrates and facilitating key bond-forming steps. Additionally, the adamantanyl groups confer steric protection around the metal center, influencing the regioselectivity and stereochemistry of the resulting products.In chemical synthesis, 1-(2-(Di(adamantan-1-yl)phosphino)phenyl)piperidine has been employed in a wide range of transformations, including cross-coupling reactions, asymmetric hydrogenation, and C-H activation processes. Its use has led to the development of efficient and selective methodologies for the construction of complex organic molecules with high levels of control over the stereochemical outcomes.Overall, the application of this unique ligand in chemical synthesis demonstrates its significance in advancing the field of catalysis and enabling the efficient preparation of valuable organic compounds with synthetic utility.