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Atomfair 1,3,5-Tri-prop-2-ynyl-[1,3,5]triazinane-2,4,6-trione C12H9N3O3

Description 1,3,5-Tri-prop-2-ynyl-[1,3,5]triazinane-2,4,6-trione (CAS No. 13185-65-4) is a highly specialized triazine derivative with the molecular formula C12H9N3O3. This compound features a symmetrical triazinane core functionalized with three prop-2-ynyl groups, offering unique reactivity for advanced organic synthesis and materials science applications. With a purity grade suitable for research and industrial use, it is supplied as a crystalline solid with documented stability under standard conditions. Its IUPAC name is 1,3,5-tris(prop-2-ynyl)-1,3,5-triazinane-2,4,6-trione , and it is also known by synonyms such as SCHEMBL1629499 and CCG-3981. Ideal for cross-coupling reactions, polymer chemistry, and pharmaceutical intermediate synthesis, this product is rigorously tested for quality assurance.

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Description

Description

1,3,5-Tri-prop-2-ynyl-[1,3,5]triazinane-2,4,6-trione (CAS No. 13185-65-4) is a highly specialized triazine derivative with the molecular formula C12H9N3O3. This compound features a symmetrical triazinane core functionalized with three prop-2-ynyl groups, offering unique reactivity for advanced organic synthesis and materials science applications. With a purity grade suitable for research and industrial use, it is supplied as a crystalline solid with documented stability under standard conditions. Its IUPAC name is 1,3,5-tris(prop-2-ynyl)-1,3,5-triazinane-2,4,6-trione, and it is also known by synonyms such as SCHEMBL1629499 and CCG-3981. Ideal for cross-coupling reactions, polymer chemistry, and pharmaceutical intermediate synthesis, this product is rigorously tested for quality assurance.

  • CAS No: 13185-65-4
  • Molecular Formula: C12H9N3O3
  • Molecular Weight: 243.22
  • Exact Mass: 243.06439116
  • Monoisotopic Mass: 243.06439116
  • IUPAC Name: 1,3,5-tris(prop-2-ynyl)-1,3,5-triazinane-2,4,6-trione
  • SMILES: C#CCN1C(=O)N(C(=O)N(C1=O)CC#C)CC#C
  • Synonyms: 1,3,5-Tri-prop-2-ynyl-[1,3,5]triazinane-2,4,6-trione, SCHEMBL1629499, ZZNPHULACRQIKD-UHFFFAOYSA-N, CCG-3981, EU-0041915

Application

This compound serves as a versatile building block in click chemistry due to its terminal alkyne groups, enabling Huisgen cycloaddition reactions for bioconjugation. Researchers utilize it in the development of triazine-based polymers with tailored thermal and mechanical properties. It is also investigated as a precursor for heterocyclic scaffolds in medicinal chemistry and agrochemical research.

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