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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-phenyl-

OC(=O)C1CCN(CC1)c1ccccc1 Request for Quotation
Chemical Name: 4-Piperidinecarboxylic acid, 1-phenyl-
CAS Number: 94201-40-8
Product Number: AG00GYJR(AGN-PC-0KO0IR)
Synonyms:
MDL No:
Molecular Formula: C12H15NO2
Molecular Weight: 205.2530

Identification/Properties

Computed Properties
Molecular Weight:
205.257g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
205.11g/mol
Monoisotopic Mass:
205.11g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
216
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-Phenyl-4-piperidinecarboxylic acid, also known as PPAC, is a versatile compound widely used in chemical synthesis. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals due to its unique structural properties. In chemical synthesis, PPAC is commonly employed as a key intermediate in the development of complex molecular structures, particularly in the formation of heterocyclic compounds. Its reactive carboxylic acid group enables it to participate in a wide array of organic reactions, including esterifications, amidations, and condensations, making it an essential tool for organic chemists seeking to generate novel compounds. Furthermore, the aromatic phenyl ring and piperidine moiety of PPAC provide additional structural diversity, allowing for the incorporation of these functional groups into tailored molecules with specific properties and activities. Overall, the application of 1-Phenyl-4-piperidinecarboxylic acid in chemical synthesis enables researchers to efficiently access diverse compound libraries and advance the discovery of new materials with potential therapeutic, agricultural, or industrial applications.