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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(1H)-Pyrazinone, 3-phenyl-

O=c1[nH]ccnc1c1ccccc1 Request for Quotation
Chemical Name: 2(1H)-Pyrazinone, 3-phenyl-
CAS Number: 2882-18-0
Product Number: AG002WNN(AGN-PC-0JPKR2)
Synonyms:
MDL No:
Molecular Formula: C10H8N2O
Molecular Weight: 172.1833

Identification/Properties

Computed Properties
Molecular Weight:
172.187g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
172.064g/mol
Monoisotopic Mass:
172.064g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
262
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Phenylpyrazin-2(1H)-one, also known as phenylpyrazinone, serves as a versatile building block in chemical synthesis due to its unique structural properties. This compound exhibits reactivity at both the phenyl ring and the pyrazinone moiety, making it highly valuable in various synthetic pathways.One key application of 3-Phenylpyrazin-2(1H)-one is as a precursor in the synthesis of pharmaceutical compounds. Its aromatic phenyl group can undergo functionalization reactions, allowing for the introduction of different substituents to modulate the biological activity of the final molecule. Additionally, the pyrazinone ring provides a scaffold for diverse molecular modifications, enabling the creation of novel drug candidates with enhanced properties.Moreover, 3-Phenylpyrazin-2(1H)-one is utilized in the preparation of agrochemicals and specialty chemicals. By incorporating this compound into synthetic routes, chemists can access a wide range of structural motifs that exhibit specific functionalities required for desired product applications. The ability to tailor the molecular structure of the final products using 3-Phenylpyrazin-2(1H)-one highlights its utility in designing advanced chemical entities with tailored properties.Overall, the strategic incorporation of 3-Phenylpyrazin-2(1H)-one in chemical synthesis enables the efficient construction of diverse organic compounds with potential applications in the pharmaceutical, agrochemical, and specialty chemical industries. Its versatility and reactivity make it a valuable building block for designing functional molecules with tailored properties.