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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)-Quinoxalinone, 7-nitro-

[O-][N+](=O)c1ccc2c(c1)[nH]c(=O)cn2 Request for Quotation
Chemical Name: 2(1H)-Quinoxalinone, 7-nitro-
CAS Number: 89898-96-4
Product Number: AG00IFVM(AGN-PC-003EIC)
Synonyms:
MDL No:
Molecular Formula: C8H5N3O3
Molecular Weight: 191.1436

Identification/Properties

Properties
MP:
275-276°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
191.146g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
191.033g/mol
Monoisotopic Mass:
191.033g/mol
Topological Polar Surface Area:
87.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
297
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-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


7-Nitro-2(1H)-quinoxalinone is a versatile compound widely used in chemical synthesis. It serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. This compound is particularly valuable in the development of novel molecules with diverse biological activities, making it a valuable tool in drug discovery and organic synthesis. Its unique structure and reactivity make it a crucial component in the creation of complex organic compounds, enabling researchers to access new chemical entities with potential therapeutic applications. In addition, 7-Nitro-2(1H)-quinoxalinone plays a crucial role in the synthesis of fluorescent dyes, polymer additives, and materials for optoelectronic devices. Its versatility and importance in chemical synthesis make it a valuable asset in the toolkit of synthetic chemists striving to push the boundaries of molecular design and innovation.