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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-(4-Chlorophenyl)piperidine-2,6-dione

O=C1CC(CC(=O)N1)c1ccc(cc1)Cl Request for Quotation
Chemical Name: 4-(4-Chlorophenyl)piperidine-2,6-dione
CAS Number: 84803-46-3
Product Number: AG008GBW(AGN-PC-0KK2FQ)
Synonyms:
MDL No:
Molecular Formula: C11H10ClNO2
Molecular Weight: 223.6556

Identification/Properties

Computed Properties
Molecular Weight:
223.656g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
223.04g/mol
Monoisotopic Mass:
223.04g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
256
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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


4-(4-Chlorophenyl)piperidine-2,6-dione is a versatile compound commonly utilized in chemical synthesis processes. This specific compound plays a crucial role in the construction of various biologically active molecules and pharmaceuticals. Its unique structure enables it to act as a key intermediate in the synthesis of complex organic compounds.In chemical synthesis, 4-(4-Chlorophenyl)piperidine-2,6-dione serves as a valuable building block for creating compounds with specific pharmacological activities. Its incorporation into synthetic pathways allows chemists to introduce functional groups and modify the molecular structure to achieve desired properties. Additionally, the presence of the piperidine ring in this compound enhances its reactivity and compatibility with a wide range of synthetic strategies.Furthermore, the chlorophenyl substituent in 4-(4-Chlorophenyl)piperidine-2,6-dione confers distinct characteristics and reaction pathways, expanding the compound's applicability in diverse synthetic schemes. This compound's involvement in chemical synthesis highlights its significance as a strategic component in the development of novel compounds with potential therapeutic applications.