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CAS RN: 1838-41-1 | Product Number: T2717
Tetramethylammonium Dichloroiodate
![Tetramethylammonium Dichloroiodate No-Image](/medias/T2717.jpg?context=bWFzdGVyfHJvb3R8NDIwNTl8aW1hZ2UvanBlZ3xhRGcyTDJnMk1DODRPVEl6TlRNNU9ETXlPRFl5TDFReU56RTNMbXB3Wnd8OTljMDBlNGI2NWY5MjY2N2I4ZWY3ZmZiODlhZmQ0YmM2ZDhlMTk0MzEyZWFhNDgxMzU1NmI3Mjg5YjcxMTllYg)
Purity: >95.0%(T)
Synonyms:
Product Documents:
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Product Number | T2717 |
Purity / Analysis Method | >95.0%(T) |
Molecular Formula / Molecular Weight | C__4H__1__2Cl__2IN = 271.95 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 1838-41-1 |
Reaxys Registry Number | 3914936 |
PubChem Substance ID | 253660202 |
MDL Number | MFCD00800939 |
Specifications
Appearance | Light yellow to Amber to Dark green powder to crystal |
Purity(Iodometric Titration) | min. 95.0 % |
Properties (reference)
Melting Point | 216 °C(dec.) |
GHS
Pictogram |
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Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
H.S.code* | 2923.90-000 |
Application
An Environmentally Friendly Iodination Reagent
Experimental procedure1): The aromatic compound (5.0 mmol) is added to tetramethylammonium dichloroiodate (1.4 g, 5.0 mmol) in a mortar. The reaction mixture is ground with a pestle to produce a homogeneous powder, and the mixture is left for 5 ~ 45 min at room temperature. When TLC shows complete disappearance of starting aromatic compound, to the brown solid is added 5 mL of sodium bisulfate (5%) and the reaction mixture is extracted with ether (3 × 5 mL). The combined extracts are dried with MgSO4. Evaporation of the solvent gives corresponding iodoaromatic derivatives. The product is purified by column chromatography on silica gel using a mixture of hexane/EtOAc (80:20).
References
- 1)Tetramethylammonium Dichloroiodate: An Efficient and Environmentally Friendly Iodination Reagent for Iodination of Aromatic Compounds under Mild and Solvent-Free Conditions
- 2)Dihaloiodates(I): synthesis with hydrogen peroxide and their halogenating activity
- 3)Total Synthesis of (±)-δ-Rubromycin
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