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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)-

Benzenesulfonamide, 4-amino-N-2-quinoxalinyl-, monosodium salt

Nc1ccc(cc1)S(=O)(=O)[N-]c1cnc2c(n1)cccc2.[Na+] Request for Quotation
Chemical Name: Benzenesulfonamide, 4-amino-N-2-quinoxalinyl-, monosodium salt
CAS Number: 967-80-6
Product Number: AG00IJUN(AGN-PC-0W6F66)
Synonyms:
MDL No:
Molecular Formula: C14H11N4NaO2S
Molecular Weight: 322.3175

Identification/Properties

Computed Properties
Molecular Weight:
322.318g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
322.05g/mol
Monoisotopic Mass:
322.05g/mol
Topological Polar Surface Area:
95.3A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
448
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Sulfaquinoxaline sodium, a potent chemical compound, plays a key role in chemical synthesis, particularly in the production of pharmaceuticals and veterinary medicines. Its application stems from its remarkable antimicrobial properties which effectively inhibit the growth of a wide range of bacteria and protozoa.When utilized in chemical synthesis, Sulfaquinoxaline sodium serves as a crucial building block in the creation of various pharmaceutical formulations. Its ability to disrupt the metabolic pathways of microorganisms makes it a valuable component in the construction of antimicrobial agents. Additionally, its solubility and stability properties make it a suitable choice for incorporating into different formulations.In the realm of pharmaceutical development, Sulfaquinoxaline sodium is often employed in the synthesis of antiprotozoal drugs due to its ability to target and combat protozoan infections effectively. Its mechanism of action involves inhibiting the synthesis of folic acid, an essential component for the survival of many microorganisms, which ultimately leads to their demise.Furthermore, Sulfaquinoxaline sodium's versatility extends to veterinary medicine, where it is utilized for the treatment and prevention of various bacterial and protozoal infections in animals. Its efficacy in controlling infections makes it a valuable tool for ensuring the health and well-being of livestock and companion animals.Overall, Sulfaquinoxaline sodium's application in chemical synthesis demonstrates its significance in the development of antimicrobial agents for both human and animal health. Its role in inhibiting the growth of harmful microorganisms underscores its importance in the field of pharmaceutical and veterinary sciences.