| Identification | Back Directory | [Name]
1,3-DIIODO-5,5-DIMETHYLHYDANTOIN | [CAS]
2232-12-4 | [Synonyms]
DIH
1,3-DIIODO-5,5-DIMET
Hydantoin Impurity 6
1,3-DIIODO-5,5-DIMETHYLHYDANTOIN
Hydantoin 1,3-Diiodo 5,5-Dimethyl
N,N'-Diiodo-5,5'-dimethylhydantoin
1,3- di iodo-5,5-dimethylhydantion
1,3-Diiodo-5,5-dimethylhydantoin>
1,3-Diiodo-5,5-dimethylhydantoin >=96%
1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione
1,3-Diiodo-5,5-dimethylimidazolidine-2,4-dione
2,4-Imidazolidinedione, 1,3-diiodo-5,5-dimethyl- | [Molecular Formula]
C5H6I2N2O2 | [MDL Number]
MFCD00020867 | [MOL File]
2232-12-4.mol | [Molecular Weight]
379.922 |
| Chemical Properties | Back Directory | [Melting point ]
198°C(dec.)(lit.) | [Boiling point ]
298.4±23.0 °C(Predicted) | [density ]
2.69±0.1 g/cm3(Predicted) | [storage temp. ]
?20°C | [form ]
powder to crystal | [pka]
-3.25±0.40(Predicted) | [color ]
White to Light yellow to Light orange | [BRN ]
146040 | [InChIKey]
RDZHCKRAHUPIFK-UHFFFAOYSA-N |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
DIH - Highly efficient and economical reagent for Iodination
Used for:
- Preparation of nitriles from corresponding alcohols and amines via oxidative conversion
- Chemoselective, stereospecific iododesilylation of silylated alkenes
- Preparation of N-benzyl toluenesulfonamides via sulfonylamidation of alkylbenzenes with toluenesulfonamide in presence of diiododimethylhydantoin
- Iodination reactions
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