Triazine derivatives consist of a six-membered aromatic ring containing three nitrogen atoms. Isomeric forms include 1,2,3-; 1,2,4-; and 1,3,5-triazine. Tri-substituted 1,3,5-triazines are one of the oldest classes of organic compounds that continue to be used as important core structures in many chemotherapeutic agents due to their interesting pharmacological properties, including anticancer, anti-angiogenesis, anti-HIV, antimalarial, antibacterial, and antimicrobial activities. These compounds have also been used as subunits in the formation of supramolecular structures because they possess good optical and electronic properties and are able to form multiple hydrogen bonds. Triazine derivatives have also been found to be PI3K and mTOR inhibitors, as well as efficient corrosion inhibitors for mild steel in acidic solutions. The presence of a halogen allows these reagents to be used as substrates in various coupling reactions, including Suzuki-Miyaura cross-coupling reactions.

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690740 Cyanuric chloride Lonza quality, ≥99.5% (w/w) C3Cl3N3
176125 Trichloroisocyanuric acid C3Cl3N3O3
91220 Trichloroisocyanuric acid technical, ≥95% (CHN) C3Cl3N3O3
711551 2-Amino-4,6-dichloro-1,3,5-triazine ≥96% C3H2Cl2N4
C33301 2-Chloro-4,6-diamino-1,3,5-triazine 95% C3H4ClN5
CBR01633 2,4-Dichloro-6-methyl-1,3,5-triazine AldrichCPR C4H3Cl2N3
213535 2,4-Dichloro-6-methoxy-1,3,5-triazine C4H3Cl2N3O
CDS002398 6-Chloro[1,2,4]triazolo[4,3-b]pyridazine AldrichCPR C5H3ClN4
375217 2-Chloro-4,6-dimethoxy-1,3,5-triazine 97% C5H6ClN3O2
CDS001555 2,4-Dichloro-6-N-propoxy-1,3,5-triazine AldrichCPR C6H7Cl2N3O
CDS009798 5-(2,4-dichloro-phenyl)-[1,2,4]triazin-3-ylamine AldrichCPR C9H6Cl2N4
762288 2-Amino-4-chloro-6-phenyl-1,3,5-triazine 95% C9H7ClN4
CDS011380 2-amino-4-(2,4-difluorophenylamino)-1,3,5-triazine AldrichCPR C9H7F2N5
597244 2,4-Diamino-6-(4-bromophenyl)-1,3,5-triazine 97% C9H8BrN5
592188 2,4-Diamino-6-(4-chlorophenyl)-1,3,5-triazine 97% C9H8ClN5
269999 Tris(2,3-dibromopropyl) isocyanurate 97% C12H15Br6N3O3