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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-Piperidinecarboxamide, N-[(4-methoxyphenyl)methyl]-

COc1ccc(cc1)CNC(=O)C1CCNCC1 Request for Quotation
Chemical Name: 4-Piperidinecarboxamide, N-[(4-methoxyphenyl)methyl]-
CAS Number: 380608-75-3
Product Number: AG0076FG(AGN-PC-0JXJRH)
Synonyms:
MDL No:
Molecular Formula: C14H20N2O2
Molecular Weight: 248.3208

Identification/Properties

Computed Properties
Molecular Weight:
248.326g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
248.152g/mol
Monoisotopic Mass:
248.152g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
257
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(4-Methoxybenzyl)piperidine-4-carboxamide, also known as $name$, is a versatile compound widely used in chemical synthesis as a key building block for the creation of various pharmaceuticals and organic compounds. Its unique molecular structure and reactivity make it ideal for a range of synthetic strategies in the laboratory.In organic synthesis, $name$ can serve as a precursor in the formation of different functional groups through chemical transformations such as acylation, alkylation, and cyclization reactions. Its piperidine core provides a valuable scaffold for the modification of drug molecules to enhance their biological activity or improve their pharmacokinetic properties.Furthermore, the presence of the methoxybenzyl group in $name$ offers opportunities for selective functionalization at specific positions, allowing chemists to fine-tune the structure of target molecules with precision. This flexibility in molecular design is crucial in the development of new drugs and therapeutic agents with enhanced efficacy and reduced side effects.Overall, the application of N-(4-Methoxybenzyl)piperidine-4-carboxamide in chemical synthesis showcases its importance as a valuable building block for the creation of novel compounds with potential therapeutic benefits in various fields of medicine and pharmaceutical research.