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Atomfair 4-Methyl-1,2,4-triazoline-3,5-dione 4-MTAD C3H3N3O2
Description 4-Methyl-1,2,4-triazoline-3,5-dione (CAS: 13362-28-2) is a highly reactive heterocyclic compound with the molecular formula C3H3N3O2. This specialized chemical, also known by its IUPAC name 4-methyl-1,2,4-triazole-3,5-dione , is widely utilized in organic synthesis and materials science due to its unique electrophilic properties. It serves as a versatile dienophile in Diels-Alder reactions, enabling the formation of complex heterocyclic frameworks with high regioselectivity. The compound is supplied as a high-purity solid, rigorously tested for quality assurance, and is ideal for researchers requiring precise and reactive intermediates for advanced synthetic applications. Proper handling under inert conditions is recommended due to its sensitivity to moisture…
Description
Description
4-Methyl-1,2,4-triazoline-3,5-dione (CAS: 13362-28-2) is a highly reactive heterocyclic compound with the molecular formula C3H3N3O2. This specialized chemical, also known by its IUPAC name 4-methyl-1,2,4-triazole-3,5-dione, is widely utilized in organic synthesis and materials science due to its unique electrophilic properties. It serves as a versatile dienophile in Diels-Alder reactions, enabling the formation of complex heterocyclic frameworks with high regioselectivity. The compound is supplied as a high-purity solid, rigorously tested for quality assurance, and is ideal for researchers requiring precise and reactive intermediates for advanced synthetic applications. Proper handling under inert conditions is recommended due to its sensitivity to moisture and air.
- CAS No: 13362-28-2
- Molecular Formula: C3H3N3O2
- Molecular Weight: 113.08
- Exact Mass: 113.022526347
- Monoisotopic Mass: 113.022526347
- IUPAC Name: 4-methyl-1,2,4-triazole-3,5-dione
- SMILES: CN1C(=O)N=NC1=O
- Synonyms: 13274-43-6, 4-Methyl-1,2,4-triazoline-3,5-dione, 3H-1,2,4-Triazole-3,5(4H)-dione, 4-methyl-, 4-Mtad, DTXSID30157738
Application
4-Methyl-1,2,4-triazoline-3,5-dione is primarily used as a dienophile in Diels-Alder reactions, facilitating the synthesis of nitrogen-containing heterocycles. It is also employed in the modification of polymers and biomolecules through cycloaddition chemistry. Researchers leverage its reactivity for labeling and crosslinking applications in proteomics and materials science.
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