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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)-

3-(4-Chlorobenzyl)-2-piperidone

O=C1NCCCC1Cc1ccc(cc1)Cl Request for Quotation
Chemical Name: 3-(4-Chlorobenzyl)-2-piperidone
CAS Number: 1260763-19-6
Product Number: AG000R67(AGN-PC-0WAGGN)
Synonyms:
MDL No:
Molecular Formula: C12H14ClNO
Molecular Weight: 223.6987

Identification/Properties

Computed Properties
Molecular Weight:
223.7g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
223.076g/mol
Monoisotopic Mass:
223.076g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
224
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


3-(4-Chlorobenzyl)-2-piperidone is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. As a key intermediate in organic chemistry, this compound serves as a building block for the creation of various complex molecules and pharmaceuticals. Its strategic placement of functional groups allows for efficient derivatization and modification, making it a valuable component in the development of new compounds.In chemical synthesis, 3-(4-Chlorobenzyl)-2-piperidone is commonly used in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its piperidone scaffold provides a versatile platform for the introduction of diverse chemical moieties, enabling the synthesis of compounds with a broad range of biological activities.Furthermore, the presence of the chlorobenzyl group in 3-(4-Chlorobenzyl)-2-piperidone enhances its reactivity and compatibility with various reaction conditions. This makes it a preferred choice for chemists seeking to introduce selective modifications or functional groups into target molecules.Overall, the application of 3-(4-Chlorobenzyl)-2-piperidone in chemical synthesis showcases its importance as a valuable building block in the creation of novel compounds with potential applications in the pharmaceutical and chemical industries.