| Identification | More | [Name]
Trimethylsulfonium iodide | [CAS]
2181-42-2 | [Synonyms]
TRIMETHYLSULFONIUM IODIDE
TRIMETHYLSULPHONIUM IODIDE
Sulfonium, trimethyl-, iodide
trimethyl-sulfoniuiodide
Trimethylsulfonium iodine
trimethylsulfone iodide
Trimethylsulfoniumiodid | [EINECS(EC#)]
218-555-4 | [Molecular Formula]
C3H9IS | [MDL Number]
MFCD00011632 | [Molecular Weight]
204.07 | [MOL File]
2181-42-2.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3 | [RTECS ]
WR8750000 | [F ]
8 | [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29309070 |
| Hazard Information | Back Directory | [Chemical Properties]
WHITE TO YELLOWISH CRYSTALLINE SOLID | [Application]
Trimethylsulfonium Iodide is a sulfoxonium salt. It is used to Treatment with strong base yields the dimethylsulfonium methylide which reacts in-situ with the carbonyl group of ketones to form epoxides or allylic alcohols. | [Uses]
Trimethylsulfonium iodide is a salt that is usually dissolved in strong base in order to synthesize epoxides in-situ. Trimethylsulfonium iodide also has the potential to inhibit human placental diamine oxidase. | [Preparation]
Trimethylsulfoxonium iodide may be prepared by the reaction of dimethyl sulfoxide and iodomethane:
(CH3)2SO + CH3I → (CH3)3SO+I | [reaction suitability]
reaction type: C-C Bond Formation | [Purification Methods]
Crystallise the iodide from EtOH. [Emeleus & Heal J Chem Soc 1126 1946, Swain & Kaiser J Am Chem Soc 80 4089 1958, Borredon et al. J Org Chem 55 501 1990, Bouda et al. Synth Commun 17 503 1987.] |
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