1. Home
  2. benzyl 3-(2-oxoethyl)piperidine-1-carboxylate

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

benzyl 3-(2-oxoethyl)piperidine-1-carboxylate

O=CCC1CCCN(C1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: benzyl 3-(2-oxoethyl)piperidine-1-carboxylate
CAS Number: 372159-77-8
Product Number: AG00CA3H(AGN-PC-078MYY)
Synonyms:
MDL No:
Molecular Formula: C15H19NO3
Molecular Weight: 261.31626

Identification/Properties

Properties
Form:
Solid

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Benzyl 3-(2-oxoethyl)piperidine-1-carboxylate is a valuable compound widely used in chemical synthesis. Specifically, it serves as a versatile building block in the creation of a variety of complex organic molecules. This compound exhibits reactivity at both the piperidine ring and the ester functionality, allowing for strategic manipulation in synthetic pathways.In chemical synthesis, Benzyl 3-(2-oxoethyl)piperidine-1-carboxylate can be utilized as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and functional groups make it valuable in the construction of heterocyclic compounds and biologically active molecules. This compound can participate in various reactions such as esterification, amidation, and cyclization, enabling the formation of diverse chemical structures with potential biological activities.Moreover, Benzyl 3-(2-oxoethyl)piperidine-1-carboxylate offers synthetic chemists the opportunity to introduce stereochemical elements into their target molecules, enhancing the complexity and diversity of organic compounds that can be accessed. Its compatibility with a range of synthetic methodologies makes it a valuable tool for designing and executing complex synthetic routes efficiently and selectively.