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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)-

2-Piperidinone, 5-hydroxy-5-methyl-

O=C1CCC(CN1)(C)O Request for Quotation
Chemical Name: 2-Piperidinone, 5-hydroxy-5-methyl-
CAS Number: 501435-45-6
Product Number: AG00DKZW(AGN-PC-0AMB8K)
Synonyms:
MDL No:
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Computed Properties
Molecular Weight:
129.159g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
129.079g/mol
Monoisotopic Mass:
129.079g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
135
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Hydroxy-5-methylpiperidin-2-one is a versatile compound widely used in chemical synthesis, particularly in the production of pharmaceuticals and fine chemicals. This cyclic compound serves as a key building block in the synthesis of various complex molecules due to its unique structure and reactivity.In chemical synthesis, 5-Hydroxy-5-methylpiperidin-2-one can act as a precursor for the synthesis of heterocyclic compounds, which are commonly found in pharmaceutical drugs. It is often utilized as a starting material in the construction of drug candidates and bioactive molecules. The hydroxy and methyl groups present in the molecule can undergo various chemical transformations, enabling the attachment of different functional groups to tailor the properties of the final product.Additionally, 5-Hydroxy-5-methylpiperidin-2-one can participate in various organic reactions such as acylation, alkylation, and condensation reactions. These reactions allow for the modification of the molecule's structure, leading to the generation of diverse compounds with potential biological activities. The presence of the piperidinone ring in the molecule imparts stability and rigidity, making it an attractive scaffold for the design of molecules with specific pharmacological profiles.Overall, the application of 5-Hydroxy-5-methylpiperidin-2-one in chemical synthesis plays a crucial role in the development of new drugs, agrochemicals, and other compounds with therapeutic benefits. Its versatility and reactivity make it a valuable intermediate in the synthesis of complex organic molecules with potential applications in various fields.