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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)-

3-Piperidinecarboxylic acid, 1-(phenylmethyl)-

OC(=O)C1CCCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 3-Piperidinecarboxylic acid, 1-(phenylmethyl)-
CAS Number: 141943-04-6
Product Number: AG001HFQ(AGN-PC-00VA65)
Synonyms:
MDL No:
Molecular Formula: C13H17NO2
Molecular Weight: 219.2796

Identification/Properties

Computed Properties
Molecular Weight:
219.284g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
219.126g/mol
Monoisotopic Mass:
219.126g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
236
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-Benzylpiperidine-3-carboxylic acid is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. In chemical synthesis, 1-Benzylpiperidine-3-carboxylic acid acts as a valuable intermediate in the production of complex molecules. Its functional groups allow for efficient and selective transformations, making it a valuable tool for chemists in creating new compounds. Additionally, the presence of the piperidine ring in the structure provides opportunities for further modification and derivatization, leading to a diverse range of potential products. This compound plays a crucial role in the development of innovative materials and chemicals through its participation in intricate synthetic pathways. Overall, the application of 1-Benzylpiperidine-3-carboxylic acid in chemical synthesis showcases its significance in the creation of valuable compounds with various industrial and scientific applications.