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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)-

Piperazine, 1-(2-pyridinylcarbonyl)-

O=C(c1ccccn1)N1CCNCC1 Request for Quotation
Chemical Name: Piperazine, 1-(2-pyridinylcarbonyl)-
CAS Number: 39639-98-0
Product Number: AG00BYJP(AGN-PC-0JNGHQ)
Synonyms:
MDL No:
Molecular Formula: C10H13N3O
Molecular Weight: 191.2297

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
191.234g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
191.106g/mol
Monoisotopic Mass:
191.106g/mol
Topological Polar Surface Area:
45.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
202
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


1-(Pyridin-2-ylcarbonyl)piperazine is a versatile compound commonly used in chemical synthesis for various applications. Its unique structure allows for a wide range of reactions and transformations, making it a valuable building block in organic chemistry. In chemical synthesis, 1-(Pyridin-2-ylcarbonyl)piperazine serves as an important intermediate in the preparation of pharmaceutical compounds, agrochemicals, and other specialty chemicals. Its presence in a molecule can enhance its biological activity, solubility, and stability, making it essential in drug discovery and development processes. Furthermore, this compound can participate in various functional group transformations, such as cross-coupling reactions, nucleophilic additions, and cyclization reactions, leading to the formation of complex molecular architectures. Its nitrogen-containing heterocyclic core also provides opportunities for diversification through further derivatization, enabling the synthesis of novel compounds with tailored properties.Overall, 1-(Pyridin-2-ylcarbonyl)piperazine plays a crucial role in modern organic synthesis, offering chemists a powerful tool for the creation of diverse and functionalized molecules with potential applications in the pharmaceutical, agricultural, and materials science industries.