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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, 6-methoxy-

COc1ccc2=NC(=O)CN=c2c1 Request for Quotation
Chemical Name: 2(1H)-Quinoxalinone, 6-methoxy-
CAS Number: 91192-32-4
Product Number: AG00IGJ5(AGN-PC-00MKN1)
Synonyms:
MDL No:
Molecular Formula: C9H8N2O2
Molecular Weight: 176.1720

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methoxyquinoxalin-2(1H)-one, a key intermediate in organic chemistry, plays a crucial role in chemical synthesis processes. This compound serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties. In synthetic chemistry, 6-Methoxyquinoxalin-2(1H)-one acts as a key reagent for the construction of complex molecular structures through various reaction pathways such as nucleophilic substitution, oxidation, and heterocyclic coupling reactions. Its ability to undergo selective functionalization makes it a valuable tool for creating diverse chemical compounds with specific properties and functionalities. Furthermore, 6-Methoxyquinoxalin-2(1H)-one's versatility and reactivity make it an indispensable component in the synthesis of novel compounds with potential applications in medicinal chemistry, materials science, and other fields of organic synthesis.