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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)-

4-Piperidinone, 1-(2-pyridinyl)-

O=C1CCN(CC1)c1ccccn1 Request for Quotation
Chemical Name: 4-Piperidinone, 1-(2-pyridinyl)-
CAS Number: 264608-41-5
Product Number: AG00CH29(AGN-PC-01UR8T)
Synonyms:
MDL No:
Molecular Formula: C10H12N2O
Molecular Weight: 176.2151

Identification/Properties

Computed Properties
Molecular Weight:
176.219g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
176.095g/mol
Monoisotopic Mass:
176.095g/mol
Topological Polar Surface Area:
33.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
183
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


1-(Pyridin-2-yl)piperidin-4-one is a versatile compound that finds wide application in chemical synthesis. It serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its unique structural characteristics, this compound can participate in a variety of chemical reactions, enabling the synthesis of complex molecules with diverse functionalities. In organic synthesis, 1-(Pyridin-2-yl)piperidin-4-one acts as a key intermediate for the construction of heterocyclic compounds and can undergo functional group transformations to introduce desired properties into target molecules. Its presence in the molecular structure imparts specific biological activities, making it a valuable tool for drug discovery and development efforts. In summary, the strategic incorporation of 1-(Pyridin-2-yl)piperidin-4-one into synthetic pathways enables chemists to access a wide range of structurally diverse compounds with potential applications in various fields.