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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-(4-pyridinylmethyl)-

O=C1CCN(CC1)Cc1ccncc1 Request for Quotation
Chemical Name: 4-Piperidinone, 1-(4-pyridinylmethyl)-
CAS Number: 126832-82-4
Product Number: AG000TB5(AGN-PC-0NE676)
Synonyms:
MDL No: MFCD05864751
Molecular Formula: C11H14N2O
Molecular Weight: 190.2417

Identification/Properties

Computed Properties
Molecular Weight:
190.246g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
190.111g/mol
Monoisotopic Mass:
190.111g/mol
Topological Polar Surface Area:
33.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
190
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-4-ylmethyl)piperidin-4-one, a versatile compound widely used in chemical synthesis, plays a crucial role as a key building block in organic chemistry. Its unique structure and reactivity make it an essential intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, this compound serves as a valuable starting material for the synthesis of complex molecules due to its ability to undergo a variety of chemical transformations. Its piperidine ring provides stability and structural rigidity, while the pyridine moiety introduces aromaticity and electron-deficient characteristics, allowing for a range of reactions and functional group modifications.The presence of a ketone group in the molecule enables diverse synthetic pathways, such as reduction, oxidation, and condensation reactions, leading to the formation of structurally diverse compounds. Additionally, the substituted piperidine ring offers opportunities for selective functionalization and stereochemical control, making 1-(Pyridin-4-ylmethyl)piperidin-4-one an indispensable tool in the synthesis of complex organic molecules with precise structural features.Overall, the strategic incorporation of 1-(Pyridin-4-ylmethyl)piperidin-4-one in chemical synthesis enables efficient access to a wide range of functionalized compounds, making it a valuable asset in the development of new materials and bioactive molecules.