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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-(4-bromobenzoyl)piperidine-4-carboxylic acid

O=C(c1ccc(cc1)Br)N1CCC(CC1)C(=O)O Request for Quotation
Chemical Name: 1-(4-bromobenzoyl)piperidine-4-carboxylic acid
CAS Number: 693237-87-5
Product Number: AG00FGDC(AGN-PC-0JXOPP)
Synonyms:
MDL No:
Molecular Formula: C13H14BrNO3
Molecular Weight: 312.1592

Identification/Properties

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


The application of 1-(4-Bromobenzoyl)piperidine-4-carboxylic acid in chemical synthesis lies in its unique structural properties that make it a versatile building block for various organic reactions. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. Specifically, the presence of the piperidine ring confers the molecule with potential biological activity, making it of interest in drug discovery and development. Additionally, the 4-bromobenzoyl group can be utilized for further functionalization through cross-coupling reactions, enabling the introduction of diverse substituents to tailor the compound's properties for specific applications. Overall, 1-(4-Bromobenzoyl)piperidine-4-carboxylic acid plays a crucial role in expanding the chemical toolbox available for organic synthesis and drug design.