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CAS RN: 1838-41-1 | Product Number: T2717
Tetramethylammonium Dichloroiodate
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Purity: >95.0%(T)
Synonyms:
Product Documents:
| Size | Unit Price | Philadelphia, PA | Portland, OR | Japan* | Quantity |
|---|---|---|---|---|---|
| 5G |
$152.00
|
Contact Us | Contact Us | 30 |
|
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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 % |
| NMR | confirm to structure |
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. 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. P302 + P352 : IF ON SKIN: Wash with plenty of soap and water. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. P362 : Take off contaminated clothing and wash before reuse. |
Related Laws:
Transport Information:
| HS Number | 2923.90.0100 |
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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