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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)-

1-Piperidinecarboxylic acid, 4-acetyl-, phenylmethyl ester

O=C(N1CCC(CC1)C(=O)C)OCc1ccccc1 Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 4-acetyl-, phenylmethyl ester
CAS Number: 160809-34-7
Product Number: AG00ANMD(AGN-PC-0267GB)
Synonyms:
MDL No:
Molecular Formula: C15H19NO3
Molecular Weight: 261.3163

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzyl 4-acetylpiperidine-1-carboxylate is a versatile compound widely used in chemical synthesis. Its unique properties make it a valuable tool in various reactions and processes in the field of chemistry. Most notably, this compound is commonly employed as a key intermediate in the synthesis of pharmaceuticals and fine chemicals.In chemical synthesis, Benzyl 4-acetylpiperidine-1-carboxylate serves as a crucial building block for creating complex organic molecules. Its structural characteristics allow for selective functional group transformations and efficient formation of new bonds. Chemists utilize this compound to introduce the piperidine ring system into target molecules, providing control over stereochemistry and reactivity in the synthesis process.Additionally, Benzyl 4-acetylpiperidine-1-carboxylate exhibits good compatibility with a wide range of reagents and reaction conditions, making it a reliable choice for synthetic chemists working on diverse projects. Whether in the development of new drug candidates or the production of specialty chemicals, the strategic incorporation of this compound enables chemists to access novel molecular structures and enhance the efficiency of their synthetic routes.