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3232-84-6
1,2,4-Triazolidine-3,5-dione

Catalog#:1P0001Y2

CAS:3232-84-6

MDL:MFCD00005225

Molecular Formula:C2H3N3O2

Molecular Weight:101.0641

UN Number:

Haz Class:

Packing Group:

Synonyms: 1,2,4-triazole-3,5-dione; urazole; 3,5-Dihydroxy-1,2,4-triazole; UNII-U4VGB8C36D; Urazole, 97%; NSC 1892; NSC 15394; U4VGB8C36D; 1H-1,2,4-Triazole-3,5(2H,4H)-dione; NSC1892; UDATXMIGEVPXTR-UHFFFAOYSA-N; 1,4-Triazolidine-3,5-dione; Urazole; 1H-1,4-Triazole-3,5(2H,4H)-dione; 1,2,4-Triazole-3,5-diol; EINECS 221-776-9; ACMC-209hsk; AI3-61104; AC1L2IYE; AC1Q6H0X; Bicarbamimide (VAN) (8CI); SCHEMBL130780; CHEMBL1996517; 1,2,4-Triazolidine-3,5-dione; DTXSID5062920; CTK1C3123; Tetrahydro-1,2,4-triazole-dione; 4h-1,2,4-triazole-3,5-diol; NSC-1892; NSC15394; ZINC6090867; ANW-27330; MFCD00005225; NSC-15394; 3232-84-6; AKOS015913604; MCULE-5611157961; KS-000015P5; NCI60_001576; ST50983471; U0045; 5-hydroxy-1,2-dihydro-3h-1,2,4-triazol-3-one; 5-hydroxy-2,4-dihydro-3h-1,2,4-triazol-3-one; J-640166; J-800168; Urazol; I14-46573; 3,2,4-triazole; C2H3N3O2; 2,4,6-Trimethylbenzyl chloride; C2-H3-N3-O2; CID72916; AR-1L7978; 2448-47-7; Bicarbamimide; Urazole bicarbamide; s-Triazole-2,5-diol; s-Triazole-3,5-diol;

Keywords: 3232-84-6,MFCD00005225,1P0001Y2,1,2,4-Triazolidine-3,5-dione,C2H3N3O2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P0001Y2 95% 1g $96.00 $72.00 In Stock USA ADD TO CART BUY NOW
1P0001Y2 95% 5g $244.00 $183.00 In Stock USA ADD TO CART BUY NOW
1P0001Y2 95% 10g $456.00 $342.00 In Stock USA ADD TO CART BUY NOW 

  •                                        1,2,4-Triazolidine-3,5-dione, also known as TAD, is a versatile compound commonly used in chemical synthesis as a valuable building block. Its unique structure and reactivity make it a key intermediate in the synthesis of various functional materials and pharmaceutical compounds. TAD is particularly valued for its ability to undergo cycloaddition reactions with a range of nucleophiles and electrophiles, yielding complex structures with high efficiency and selectivity. In organic synthesis, TAD can act as a masked form of ketene, enabling the introduction of ketene functionalities under mild conditions. Furthermore, TAD can participate in diverse transformations such as cyclopropanation, nucleophilic addition, and ring-opening reactions, offering synthetic chemists a plethora of tools for constructing complex molecular scaffolds. Its broad applicability and ease of manipulation make 1,2,4-Triazolidine-3,5-dione a valuable addition to any chemist's toolkit in the pursuit of innovative and efficient chemical synthesis.

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