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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-fluoro-

Fc1ccc2c(c1)ncc(=O)[nH]2 Request for Quotation
Chemical Name: 2(1H)-Quinoxalinone, 6-fluoro-
CAS Number: 55687-23-5
Product Number: AG00DKTX(AGN-PC-0NJW7G)
Synonyms:
MDL No:
Molecular Formula: C8H5FN2O
Molecular Weight: 164.1365

Identification/Properties

Properties
MP:
300-302°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
164.139g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
164.039g/mol
Monoisotopic Mass:
164.039g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
229
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Fluoroquinoxalin-2(1H)-one is a highly versatile compound widely employed in chemical synthesis. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and materials due to its unique chemical properties.In organic synthesis, 6-Fluoroquinoxalin-2(1H)-one is utilized as a precursor for the synthesis of various heterocyclic compounds. Its fluorine substituent enhances the reactivity of the molecule, enabling selective functionalization at specific positions. This compound is particularly valuable in the development of novel drug candidates, where its presence can impart desirable pharmacological properties or improve bioavailability.Additionally, 6-Fluoroquinoxalin-2(1H)-one can participate in a range of key chemical transformations such as oxidation, reduction, and nucleophilic substitution reactions. These reactions allow for the introduction of diverse functional groups, expanding the structural diversity of synthesized molecules.Overall, the application of 6-Fluoroquinoxalin-2(1H)-one in chemical synthesis plays a crucial role in the production of valuable compounds with potential applications in various industries, making it a valuable tool for synthetic chemists.