Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Recueil de Medecine Veterinaire called Anticoccidial power of sulfachlorpyrazine (Esb 3) against Eimeria acervulina, Author is Yvore, P.; Peloille, Michele; Jacquemot, Catherine, which mentions a compound: 23307-72-4, SMILESS is ClC1=CN=CC([N-]S(=O)(C2=CC=C(N)C=C2)=O)=N1.[Na+], Molecular C10H8ClN4NaO2S, Name: Sodium ((4-aminophenyl)sulfonyl)(6-chloropyrazin-2-yl)amide.
Sulfachloropyrid-azine has the advantages of the greater efficiency and less toxicity compared with sulphaquinoxaline and sulphamethazine. With 300 mg./l. drinking water a significant anticoccidial activity in the chicken was observed and with 600 mg./l. for 5 days (administration during 3 days, no treatment during 4 days and retreatment for 2 days) no toxic effects were observed. Low doses seem to have coccidiocidal activity on 2nd schizogony. The new anticoccidial derivatives of hydroxyquinoline do not produce any immunity. Particularly E. tenella may develop again after the chemotherapy. It is possible that a complementary treatment by a sulfonamide in the drinking water during the days following the treatment may produce immunity. For this a coccidiocidal and not a coccidiostatic action should be achieved.
After consulting a lot of data, we found that this compound(23307-72-4)Name: Sodium ((4-aminophenyl)sulfonyl)(6-chloropyrazin-2-yl)amide can be used in many types of reactions. And in most cases, this compound has more advantages.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com