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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-Piperidinecarboxylicacid, 1-(4-pyridinylmethyl)-

OC(=O)C1CCN(CC1)Cc1ccncc1 Request for Quotation
Chemical Name: 4-Piperidinecarboxylicacid, 1-(4-pyridinylmethyl)-
CAS Number: 774531-43-0
Product Number: AG005LLB(AGN-PC-0KKOG8)
Synonyms:
MDL No:
Molecular Formula: C12H16N2O2
Molecular Weight: 220.2676

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
220.272g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
220.121g/mol
Monoisotopic Mass:
220.121g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
231
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


The 1-(Pyridin-4-ylmethyl)piperidine-4-carboxylic acid, also known as $name$, serves as a valuable tool in chemical synthesis. This compound is frequently employed as a building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it an essential component in the development of novel molecules with diverse applications. In chemical synthesis, $name$ can be utilized to introduce the pyridine moiety and the piperidine ring into target compounds, thereby influencing their biological activity or physical properties. Its strategic placement within a molecular framework allows for precise control over the structure-activity relationships of the final products, making it an indispensable intermediate in the synthesis of complex organic molecules.