Description

2,4,6-Tris(3,5-dimethylpyrazol-1-yl)-1,3,5-triazine (CAS No. 154403-27-7) is a highly specialized heterocyclic compound with the molecular formula C₁₈H₂₁N₉. This triazine-based ligand features three 3,5-dimethylpyrazole groups symmetrically arranged around a central 1,3,5-triazine core, making it an excellent candidate for coordination chemistry and catalysis research. With a molecular weight of 363.42 g/mol, this compound is typically supplied as a high-purity solid, ensuring consistency for advanced synthetic applications. Its unique structure allows for versatile binding to transition metals, making it valuable in the development of novel catalysts, metal-organic frameworks (MOFs), and supramolecular assemblies. Ideal for researchers in organometallic chemistry, material science, and pharmaceutical synthesis, this product is rigorously tested for quality and stored under optimal conditions to guarantee performance.

Properties

• CAS Number: 154403-27-7
• Complexity: 436
• IUPAC Name: 2,4,6-tris(3,5-dimethylpyrazol-1-yl)-1,3,5-triazine
• InChI: InChI=1S/C18H21N9/c1-10-7-13(4)25(22-10)16-19-17(26-14(5)8-11(2)23-26)21-18(20-16)27-15(6)9-12(3)24-27/h7-9H,1-6H3
• InChI Key: DGBHCVCPUCYWEM-UHFFFAOYSA-N
• Exact Mass: 363.19199171
• Molecular Formula: C18H21N9
• Molecular Weight: 363.4
• SMILES: CC1=CC(=NN1C2=NC(=NC(=N2)N3C(=CC(=N3)C)C)N4C(=CC(=N4)C)C)C
• Topological: 92.1
• Monoisotopic Mass: 363.19199171
• Synonyms: 154403-27-7, 2,4,6-tris(3,5-dimethylpyrazol-1-yl)-1,3,5-triazine, 1,3,5-Triazine, 2,4,6-tris(3,5-dimethyl-1H-pyrazol-1-yl)-, 2,4,6-Tris(3,5-dimethyl-1H -pyrazol-1-yl)-1,3,5-triazine, 2,4,6-tris(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazine, NSC669396, YSWG345, SCHEMBL4138642, CHEMBL1996358, DTXSID70327599, MFCD34473807, NSC-669396, NCI60_024211, CS-0170515, G64807, 2,4,6-tris(3,5-dimethylpyrazolyl)-1,3,5-triazine

Application

2,4,6-Tris(3,5-dimethylpyrazol-1-yl)-1,3,5-triazine is widely used as a multidentate ligand in transition metal catalysis, enabling the synthesis of complex organometallic compounds. Its rigid triazine core and pyrazole arms make it suitable for constructing stable coordination polymers and MOFs with tailored porosity. Researchers also employ this compound in the development of homogeneous catalysts for organic transformations, such as C-C coupling reactions. Additionally, its nitrogen-rich structure lends itself to applications in energetic materials and supramolecular chemistry.

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