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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)-

6-Quinoxalinecarboxylic acid

OC(=O)c1ccc2c(c1)nccn2 Request for Quotation
Chemical Name: 6-Quinoxalinecarboxylic acid
CAS Number: 6925-00-4
Product Number: AG003U3S(AGN-PC-0JURPS)
Synonyms:
MDL No:
Molecular Formula: C9H6N2O2
Molecular Weight: 174.1561

Identification/Properties

Properties
MP:
250 °C
BP:
355.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
174.159g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
174.043g/mol
Monoisotopic Mass:
174.043g/mol
Topological Polar Surface Area:
63.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
208
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-Quinoxalinecarboxylic acid, also known as quinoxalic acid, is a versatile compound that plays a crucial role in chemical synthesis. Its unique structure and properties make it a key ingredient in various chemical reactions and processes.In chemical synthesis, 6-Quinoxalinecarboxylic acid is commonly used as a building block for the construction of heterocyclic compounds. Its presence as a core structure in molecules enables the formation of diverse chemical derivatives with specific functionalities and properties. Furthermore, it serves as a valuable substrate in the preparation of pharmaceuticals, agrochemicals, dyes, and other fine chemicals.The functional groups present in 6-Quinoxalinecarboxylic acid facilitate its efficient participation in synthetic transformations such as condensation reactions, redox reactions, and substitution reactions. Its ability to undergo various chemical modifications makes it a versatile precursor for the synthesis of complex organic molecules.Overall, the application of 6-Quinoxalinecarboxylic acid in chemical synthesis showcases its significance as a fundamental component in the creation of novel compounds with tailored properties and functionalities.