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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)-

(S)-2-(Piperidin-2-yl)pyridine

C1CC[C@H](NC1)c1ccccn1 Request for Quotation
Chemical Name: (S)-2-(Piperidin-2-yl)pyridine
CAS Number: 46041-69-4
Product Number: AG00DLIE(AGN-PC-0WAITL)
Synonyms:
MDL No:
Molecular Formula: C10H14N2
Molecular Weight: 162.2316

Identification/Properties

Computed Properties
Molecular Weight:
162.236g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
162.116g/mol
Monoisotopic Mass:
162.116g/mol
Topological Polar Surface Area:
24.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
136
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-2-(piperidin-2-yl)pyridine molecule plays a crucial role in chemical synthesis as a versatile building block. This compound is highly sought after for its ability to serve as a chiral ligand in asymmetric catalysis, aiding in the formation of enantiopure products with high stereochemical control. Its presence facilitates various organic transformations, such as asymmetric hydrogenation, C–C bond formation, and other key reactions in the synthesis of complex molecules. In addition, (S)-2-(piperidin-2-yl)pyridine can also act as a coordinating ligand in transition metal-catalyzed processes, enabling the selective activation of substrates and enhancing the efficiency of the desired chemical transformations. This unique compound thus stands as a valuable tool for chemists seeking to achieve precise and controlled synthesis in their research and development endeavors.