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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)-

Piperazinone, 3-ethyl-

CCC1NCCNC1=O Request for Quotation
Chemical Name: Piperazinone, 3-ethyl-
CAS Number: 90485-52-2
Product Number: AG00GSMG(AGN-PC-0JYHCA)
Synonyms:
MDL No:
Molecular Formula: C6H12N2O
Molecular Weight: 128.1723

Identification/Properties

Properties
BP:
296.6 °C at 760 mmHg
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
128.175g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
128.095g/mol
Monoisotopic Mass:
128.095g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
114
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Ethylpiperazin-2-one is a versatile compound commonly utilized in chemical synthesis for its reactivity and functional group manipulation capabilities. In organic chemistry, it serves as a valuable building block for the synthesis of various heterocyclic compounds, pharmaceuticals, and agrochemicals. With its unique molecular structure, 3-Ethylpiperazin-2-one can participate in several key reactions such as nucleophilic substitution, oxidation, and acylation, making it a valuable intermediate in the preparation of complex organic molecules. Additionally, this compound can be functionalized to introduce specific chemical groups, enabling the fine-tuning of molecular properties for targeted applications. In summary, 3-Ethylpiperazin-2-one plays a crucial role in the synthesis of diverse chemical compounds, showcasing its significance in the field of organic chemistry and chemical research.