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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-Piperidinecarboxaldehyde, 1-phenyl-

O=CC1CCN(CC1)c1ccccc1 Request for Quotation
Chemical Name: 4-Piperidinecarboxaldehyde, 1-phenyl-
CAS Number: 111153-74-3
Product Number: AG0082W0(AGN-PC-00O72O)
Synonyms:
MDL No:
Molecular Formula: C12H15NO
Molecular Weight: 189.2536

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Phenylpiperidine-4-carbaldehyde is a versatile compound with valuable applications in chemical synthesis. As a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals, this compound serves as a building block in the creation of various complex molecules. Its reactive aldehyde group allows for the introduction of diverse functional groups, enabling chemists to tailor the structure of target compounds with precision. In addition, 1-Phenylpiperidine-4-carbaldehyde plays a crucial role in the synthesis of heterocyclic compounds, which are widely utilized in drug discovery and materials science. Its significance lies in its ability to facilitate the formation of carbon-carbon and carbon-nitrogen bonds, thereby expanding the scope of synthetic possibilities in organic chemistry. By incorporating 1-Phenylpiperidine-4-carbaldehyde into synthetic routes, researchers can access novel chemical entities with enhanced biological activity or unique properties for various applications in the fields of medicine, agriculture, and materials engineering.