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1248676-71-2

1248676-71-2 Structure

1248676-71-2 Structure
IdentificationBack Directory
[Name]

4,5-diiodo-1-methyl-triazole
[CAS]

1248676-71-2
[Synonyms]

4,5-diiodo-1-methyl-triazole
4,5-Diiodo-1-methyl-1H-1,2,3-triazole
1H-1,2,3-Triazole, 4,5-diiodo-1-methyl-
[Molecular Formula]

C3H3I2N3
[MOL File]

1248676-71-2.mol
[Molecular Weight]

334.89
Chemical PropertiesBack Directory
[Melting point ]

186-188 °C
[Boiling point ]

344.4±52.0 °C(Predicted)
[density ]

3.14±0.1 g/cm3(Predicted)
[pka]

-2.70±0.10(Predicted)
Hazard InformationBack Directory
[Description]

The chemical formula of 4,5-diiodo-1-methyl-triazole is C3H3I2N3. It can be synthesized by alkylation of 4,5-diiodo-[1H]-1,2,3-triazole. It is a derivative of 1,2,3-triazole ring which is a moiety present in anti-allergic, antibacterial, antifungal, anti-virial, and analgesic drugs
[Uses]

4,5-diiodo-1-methyl-triazole is an organic reagent capable of synthesizing a wide range of chemicals as a raw material. For example, by refluxing in 100% nitric acid, nitration of 4,5-diiodo-1-methyl-triazole was successful in forming 1-Methyl-4-nitro-5-iodo-1,2,3-triazole.
[Preparation]

4,5-Diiodo-1,2,3-[1H]-triazole (14.6 mmol, 4.7 g) was dissolved in DMF (5 mL) and potassium carbonate (23.15 mmol, 3.2g) was added. The mixture was cooled to -20 °C in an ice-salt bath. Iodomethane (21.8 mmol, 1.36 mL) was added to the cooled mixture and stirred for two hours. An off-white precipitate was formed which was filtered and washed with water. After purification, 4,5-diiodo-1-methyl-triazole can be obtained[1].
4,5-diiodo-1-methyl-triazole
[References]

[1] Chand D, et al. Mono‐ and Diiodo‐1,2,3‐Triazoles and Their Mono Nitro Derivatives. Dalton Transactions, 2016; 45: 9684-9688.
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