Methyltrifluormethansulfonat

Bezeichnung:Methyltrifluormethansulfonat

CAS-Nr333-27-7

Englisch Name:Methyl trifluoromethanesulfonate

CBNumberCB9131563

SummenformelC2H3F3O3S

Molgewicht164.1

MOL-Datei333-27-7.mol

Synonyma

Methyltrifluormethansulfonat

Methyltrifluormethansulfonat physikalisch-chemischer Eigenschaften

Siedepunkt	94-99 °C(lit.)
Dichte	1.45 g/mL at 25 °C(lit.)
Brechungsindex	n20/D 1.326(lit.)
Flammpunkt	101 °F
storage temp.	2-8°C
Löslichkeit	Chloroform (Sparingly), Ethyl Acetate (Slightly)
Aggregatzustand	Liquid
Wichte	1.450
Farbe	Clear colorless to yellow
Sensitive	Air Sensitive
BRN	774772
Stabilität	Hygroscopic, Moisture Sensitive, Volatile
InChI	InChI=1S/C2H3F3O3S/c1-8-9(6,7)2(3,4)5/h1H3
InChIKey	OIRDBPQYVWXNSJ-UHFFFAOYSA-N
SMILES	C(F)(F)(F)S(OC)(=O)=O
CAS Datenbank	333-27-7(CAS DataBase Reference)
EPA chemische Informationen	Methyl trifluoromethanesulfonate (333-27-7)

Sicherheit

Kennzeichnung gefährlicher	C,T
R-Sätze:	10-34-20/21/22
S-Sätze:	26-36/37/39-45-16
RIDADR	UN 2920 8/PG 2
WGK Germany	3
F	10
Hazard Note	Highly Toxic/Corrosive
TSCA	T
HazardClass	3.2
PackingGroup	III
HS Code	29049020

Gefahreninformationscode (GHS)

Methyl trifluoromethanesulfonate Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R10:Entzündlich.
R34:Verursacht Verätzungen.
R20/21/22:Gesundheitsschädlich beim Einatmen,Verschlucken und Berührung mit der Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S16:Von Zündquellen fernhalten - Nicht rauchen.
Chemische Eigenschaften
clear colourless to yellow liquid
Verwenden
Methyl trifluoromethanesulfonate is used as a powerful methylating reagent in chemistry. Further, it is used in the conversion of amines to methyl ammonium triflates. In addition, it is also used in Suzuki reaction.
Application
Methyl trifluoromethanesulfonate, a methylating agent, is commonly used for the pre-methylation of polysaccharides under mild basic conditions.
In the determination of polysulfides, zerovalent sulfur in sulfide-rich water wells, and polysulfide species in electrolyte of a lithium–sulfur battery using chromatography-based techniques.
In reactions with potassium enolates.
For the conversion of amines to methyl ammonium triflates.
Additionally, methyl trifluoromethanesulfonate has been utilized in the production of 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate.
Allgemeine Beschreibung
Methyl trifluoromethane sulfonate is a brown liquid. Insoluble in water. (NTP, 1992) This material is a very reactive methylating agent, also known as methyl triflate.
Air & Water Reaktionen
Highly flammable. Insoluble in water.
Reaktivität anzeigen
Methyl trifluoromethanesulfonate is sensitive to heat. . Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Health Hazard
ACUTE/CHRONIC HAZARDS: When heated to decomposition Methyl trifluoromethanesulfonate emits toxic fumes.
Brandgefahr
Methyl trifluoromethanesulfonate is combustible.
Toxikologie
Methyl trifluoromethanesulfonate is extremely hazardous. All possible precautions should be taken to avoid inhalation or absorption through the skin. This material is extremely destructive to the tissue of the mucous membranes and upper respiratory tract, eyes, and skin. Inhalation may be fatal as a result of spasm, inflammation, and edema of the larynx and bronchi, chemical pneumonitis, and pulmonary edema. Use in a fume hood. Although there has yet to be a reported human fatality, several cases were reported for methyl fluorosulfonate (LC50 (rat, 1 h) = 5 ppm), and methyl triflate is expected to have similar toxicity based on available evidence.
Synthese
Methyl trifluoromethanesulfonate is commercially available, however it may also be prepared in the laboratory by treating dimethyl sulfate with triflic acid.
CF3SO2OH + (CH3O)2SO2 → CF3SO2OCH3 + CH3OSO2OH
läuterung methode
Methyl trifluoromethanesulfonate (methyl triflate) [333-27-7] M 164.1, b 97 -97.5o/736mm, 9 9o/~760mm, 100-102o/~760mm, d 4 1.496, n D 1.3238. It is a strong methylating agent but is corrosive and POISONOUS. Fractionate it carefully and collecting the middle fraction (use an efficient fume cupboard) and keep away from moisture. It is a POWERFUL ALKYLATING AGENT and a strong IRRITANT. [IR: Gramstad & Haszeldine J Chem Soc 173 1956 , J Chem Soc 4069 1957 .] Trifluoromethanesulfonic acid (triflic acid) [1493-13-6] M 151.1, boils higher (b 162o/atm), has a pKa of 3.10, and is TOXIC and hygroscopic. [Hansen J Org Chem 30 4322 1965, Kurz & El-Nasr J Am Chem Soc 104 5823 1982, Beilstein 3 IV 34.]

Methyl trifluoromethanesulfonate Upstream-Materialien And Downstream Produkte

Methyltrifluormethansulfonat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

333-27-7, Methyl trifluoromethanesulfonate Verwandte Suche:

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