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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, 6,7-dichloro-

Oc1cnc2c(n1)cc(c(c2)Cl)Cl Request for Quotation
Chemical Name: 2(1H)-Quinoxalinone, 6,7-dichloro-
CAS Number: 78470-95-8
Product Number: AG005LWQ(AGN-PC-001DX0)
Synonyms:
MDL No:
Molecular Formula: C8H4Cl2N2O
Molecular Weight: 215.0362

Identification/Properties

Properties
BP:
429.7 °C at 760 mmHg
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
215.033g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
213.97g/mol
Monoisotopic Mass:
213.97g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
257
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#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,7-Dichloroquinoxalin-2(1H)-one is a versatile compound widely utilized in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. With its unique structure and reactivity, this compound serves as a key building block for the synthesis of various biologically active compounds.In organic chemistry, 6,7-Dichloroquinoxalin-2(1H)-one is commonly employed as a precursor in the development of pharmaceuticals due to its ability to participate in a range of synthetic transformations. Its halogen substituents can undergo diverse chemical reactions, enabling the introduction of different functional groups into the molecule. This flexibility allows for the creation of new compounds with modified properties or enhanced biological activities.Moreover, 6,7-Dichloroquinoxalin-2(1H)-one plays a crucial role in the synthesis of heterocyclic compounds, which are prevalent in many biologically active molecules. By serving as a starting material for the construction of complex ring structures, this compound contributes to the development of novel drug candidates and agrochemicals. Its use in chemical synthesis enables researchers to access diverse chemical space and explore a wide range of potential applications in the field of medicinal chemistry and agriculture.