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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-Piperidinol, 1-(4-pyridinyl)-

OC1CCN(CC1)c1ccncc1 Request for Quotation
Chemical Name: 4-Piperidinol, 1-(4-pyridinyl)-
CAS Number: 130658-65-0
Product Number: AG000UR8(AGN-PC-043BZP)
Synonyms:
MDL No:
Molecular Formula: C10H14N2O
Molecular Weight: 178.2310

Identification/Properties

Computed Properties
Molecular Weight:
178.235g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
178.111g/mol
Monoisotopic Mass:
178.111g/mol
Topological Polar Surface Area:
36.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
149
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-yl)piperidin-4-ol is a versatile compound that serves as a valuable building block in chemical synthesis. It plays a crucial role in the development of pharmaceuticals, agrochemicals, and various other fine chemicals. This compound is commonly used as a key intermediate in the synthesis of diverse organic compounds due to its unique chemical properties and functional groups.In chemical synthesis, 1-(Pyridin-4-yl)piperidin-4-ol is utilized as a precursor in the formation of complex molecules through various synthetic routes. Its piperidine ring provides a stable scaffold for further functionalization, allowing for the introduction of different substituents and modifications to tailor the properties of the final product. The presence of the pyridine moiety further enhances the reactivity and selectivity of reactions involving this compound.Moreover, 1-(Pyridin-4-yl)piperidin-4-ol can participate in a range of chemical transformations such as nucleophilic additions, substitutions, and oxidative processes, making it a versatile starting material for the synthesis of diverse organic compounds. Its ability to undergo these reactions under mild conditions contributes to its utility in the development of various chemical entities with desired biological or physical properties.Overall, the application of 1-(Pyridin-4-yl)piperidin-4-ol in chemical synthesis offers a pathway to access structurally diverse molecules with potential applications in drug discovery, material science, and other fields requiring the creation of novel compounds.