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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, 3-hydroxy-

O=C1NCCCC1O Request for Quotation
Chemical Name: 2-Piperidinone, 3-hydroxy-
CAS Number: 19365-08-3
Product Number: AG0037NF(AGN-PC-00O94J)
Synonyms:
MDL No:
Molecular Formula: C5H9NO2
Molecular Weight: 115.1305

Identification/Properties

Properties
MP:
134-136°C
BP:
352.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
115.132g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
115.063g/mol
Monoisotopic Mass:
115.063g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
103
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Hydroxy-2-piperidinone, also known as lactamin, is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. One key application of 3-hydroxy-2-piperidinone is its role as a chelating agent in metal coordination chemistry. Due to the presence of the hydroxyl and carbonyl functional groups, this compound has a high affinity for metal ions such as iron, copper, and zinc. This property makes it effective in metal ion sequestration and removal from aqueous solutions.Additionally, 3-hydroxy-2-piperidinone can act as a versatile intermediate in the synthesis of heterocyclic compounds. Its cyclic structure and functional groups allow for various chemical modifications, enabling the creation of complex molecular structures with specific biological or chemical properties.Furthermore, 3-hydroxy-2-piperidinone can serve as a precursor for the synthesis of pharmaceutical compounds with therapeutic properties. By incorporating this compound into the molecular structure of drug candidates, chemists can enhance their efficacy, bioavailability, or solubility, leading to the development of novel pharmaceutical agents with improved performance.Overall, the diverse applications of 3-hydroxy-2-piperidinone in chemical synthesis highlight its importance as a valuable tool in the creation of functional molecules for various industrial and scientific purposes.