Trimethylsulfonium iodide

Trimethylsulfonium iodide Basic information
Product Name:Trimethylsulfonium iodide
Synonyms:Trimethylsulfonium iodine;trimethylsulfone iodide;Trimethylsulfoniumiodid;Trimethylsulfonium iodide,98%;Trimethylsulfonium iodide ,99.5%;Trimethylsulphonium Iodide 99%;triMethylsulfaniuM iodide;TriMethylsulfoniuM iodide, 98% 100GR
CAS:2181-42-2
MF:C3H9IS
MW:204.07
EINECS:218-555-4
Product Categories:C-C Bond Formation;OthersOrganic Building Blocks;Iodonium Sulfonium & Oxonium Compounds;Sulfonium/Sulfoxonium Compounds;Sulfur Compounds;Synthetic Reagents;Sulfonium Compounds;Isoquinolines ,Furans ,Quinolines ,Quinaldines
Mol File:2181-42-2.mol
Trimethylsulfonium iodide Structure
Trimethylsulfonium iodide Chemical Properties
Melting point 215-220 °C (lit.)
density 1.6554 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Soluble in water, alcohol, THF, DMSO
form Crystalline Powder, Crystals and/or Chunks
color White to yellow
Water Solubility soluble
Sensitive Light Sensitive
BRN 3555192
Exposure limitsACGIH: TWA 0.01 ppm
InChIKeyVFJYIHQDILEQNR-UHFFFAOYSA-M
CAS DataBase Reference2181-42-2(CAS DataBase Reference)
NIST Chemistry ReferenceTrimethylsulfonium iodide(2181-42-2)
EPA Substance Registry SystemTrimethylsulfonium iodide (2181-42-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS WR8750000
8
TSCA Yes
HazardClass IRRITANT
HS Code 29309070
MSDS Information
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Trimethylsulfonium iodide Usage And Synthesis
Chemical Propertieswhite to yellowish crystalline solid. Soluble in water, alcohol, tetrahydrofuran, dimethyl sulfoxide.
UsesTrimethylsulfonium 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.
ApplicationTrimethylsulfonium 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.
PreparationTrimethylsulfoxonium iodide may be prepared by the reaction of dimethyl sulfoxide and iodomethane:
(CH3)2SO + CH3I → (CH3)3SO+I
After standing overnight, the resulting solid white cake is crushed and recrystallized from absolute ethanol to give pure trimethylsulfonium iodide.
Purification MethodsCrystallise 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.]
Trimethylsulfonium iodide, oxide Iodotrimethylsilane TRIMETHYLSILANE S-ADENOSYL-L-METHIONINE IODIDE SALT TRIETHYLSULFONIUM IODIDE DODECYLDIMETHYLSULFONIUM IODIDE Ammonium, 7,7,14,21,21-pentaethyl-7,21-diazonia -14-thioniaheptacosyle nebis(triethyl-, pentaiodide Sulfonium, dimethylisopentyl-, iodide L-METHIONINE METHYLSULFONIUM IODIDE TRIMETHYL-D9-SULFONIUM IODIDE Sulfonium, (3-cyclohexyl-3-hydroxy-3-phenylpropyl)dimethyl-, iodide Trimethylsulfonium iodide Diethylmethylsulfonium iodide mercuric iodide addition compound Sulfonium, (ethylmethyl)octadecyl-, iodide Tris(hydroxymethyl)aminomethane TRI-N-BUTYLSULFONIUM IODIDE Propidium iodide TRIMETHYLSULFONIUM

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