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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)-

Quinoxaline, 2,3-dichloro-6-nitro-

[O-][N+](=O)c1ccc2c(c1)nc(c(n2)Cl)Cl Request for Quotation
Chemical Name: Quinoxaline, 2,3-dichloro-6-nitro-
CAS Number: 2379-60-4
Product Number: AG00I4LS(AGN-PC-0JUYXW)
Synonyms:
MDL No:
Molecular Formula: C8H3Cl2N3O2
Molecular Weight: 244.0343

Identification/Properties

Computed Properties
Molecular Weight:
244.031g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
242.96g/mol
Monoisotopic Mass:
242.96g/mol
Topological Polar Surface Area:
71.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
261
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H318-H335
Precautionary Statements:
P261-P280-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dichloro-6-nitroquinoxaline is a versatile chemical compound widely used in organic synthesis processes. It serves as a key building block in the creation of various nitrogen-containing compounds with diverse applications in the fields of pharmaceuticals, agrochemicals, and materials science. This compound is particularly valued for its ability to introduce nitro and chloro substituents into molecular structures, allowing for the modification of functional groups and tuning of properties. In chemical synthesis, 2,3-Dichloro-6-nitroquinoxaline is utilized as a reagent in the preparation of pharmacologically active compounds and complex organic molecules with tailored properties. Its strategic role in the synthesis of biologically relevant compounds makes it an essential tool for research and development in the pharmaceutical and chemical industries.