Description

1,3,5-Triazine, 2,4-dichloro-6-(methylthio)- (CAS No. 13705-05-0) is a high-purity chlorinated triazine derivative with the molecular formula C₄H₃Cl₂N₃S. This compound, also known by its IUPAC name 2,4-dichloro-6-methylsulfanyl-1,3,5-triazine, is a versatile intermediate in organic synthesis and agrochemical applications. Its unique triazine core, functionalized with reactive chloro and methylthio groups, makes it a valuable building block for the development of herbicides, fungicides, and other specialty chemicals. The product is supplied as a crystalline solid with ≥95% purity (HPLC), ensuring consistency for research and industrial use. Proper handling under inert conditions is recommended due to its moisture-sensitive nature. Available in scalable quantities with customizable packaging options.

Properties

• CAS Number: 13705-05-0
• Complexity: 105
• IUPAC Name: 2,4-dichloro-6-methylsulfanyl-1,3,5-triazine
• InChI: InChI=1S/C4H3Cl2N3S/c1-10-4-8-2(5)7-3(6)9-4/h1H3
• InChI Key: MWPZLWRHHPWTFS-UHFFFAOYSA-N
• Exact Mass: 194.9424737
• Molecular Formula: C4H3Cl2N3S
• Molecular Weight: 196.06
• SMILES: CSC1=NC(=NC(=N1)Cl)Cl
• Topological: 64
• Monoisotopic Mass: 194.9424737
• Synonyms: 2,4-Dichloro-6-(methylthio)-1,3,5-triazine, 1,3,5-Triazine, 2,4-dichloro-6-(methylthio)-, Methylmercaptodichlorotriazine, EINECS 237-239-7, BRN 0135424, 2,4-Dichloro-6-(methylthio)-s-triazine, s-Triazine, 2,4-dichloro-6-(methylthio)-, DTXSID8065587, 4-26-00-00332 (Beilstein Handbook Reference), DTXCID8034403, 237-239-7, 13705-05-0, 2,4-dichloro-6-methylsulfanyl-1,3,5-triazine, MFCD01679001, 2,4-Dichloro-6-methylthio-1,3,5-triazine, 2-methylthio-4,6-dichloro-1,3,5-triazine, 1,3,5-Triazine,2,4-dichloro-6-(methylthio)-, SCHEMBL6765323, AKOS012166723, 2-methylmercapto-4,6-dichloro-s-triazine, AS-31777, DA-19026, SY019326, CS-0150100, NS00024446, 2 pound not4-Dichloro-6-(methylthio)-1 pound not3 pound not5-triazine

Application

This compound is primarily used as a key intermediate in the synthesis of s-triazine herbicides, such as methylthio-substituted triazine derivatives. It serves as a precursor for the development of crop protection agents targeting broadleaf weeds in corn and cereal fields. Researchers also utilize it in heterocyclic chemistry studies to explore novel sulfur-containing triazine analogs. Its reactivity enables functionalization at the chloro positions for further derivatization in pharmaceutical or material science applications.

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