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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-Piperidinecarboxylic acid, 1-(2-pyridinylmethyl)-

OC(=O)C1CCN(CC1)Cc1ccccn1 Request for Quotation
Chemical Name: 4-Piperidinecarboxylic acid, 1-(2-pyridinylmethyl)-
CAS Number: 193538-28-2
Product Number: AG00APIQ(AGN-PC-0KUMYC)
Synonyms:
MDL No:
Molecular Formula: C12H16N2O2
Molecular Weight: 220.2676

Identification/Properties

Properties
BP:
369.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
220.272g/mol
XLogP3:
-1.5
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:
237
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 1-(Pyridin-2-ylmethyl)piperidine-4-carboxylic acid is a versatile compound that finds its application in various chemical synthesis processes. With its unique structure, this compound serves as a valuable building block in the creation of diverse chemical compounds. By utilizing its piperidine backbone and pyridine moiety, chemists can introduce specific functional groups and stereochemical elements into their target molecules. This compound is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials due to its ability to impart desired properties and reactivity. Its presence in the synthesis pathway can enable the formation of intricate molecular structures, making it an indispensable tool in the hands of synthetic chemists.