Substance
ID:336654
Names and Identifiers
IUPAC name
silver(1+) ion trifluoromethanesulfonate
IUPAC Traditional name
silver(1+) ion triflate
Synonyms
Silver triflateTrifluoromethanesulfonic acid silver salt三氟甲磺酸 银盐三氟甲磺酸银Silver trifluoromethanesulfonate三氟甲烷磺酸银
Registration numbers
MDL Number
CAS Number
EC Number
Beilstein Number
PubChem SID
Properties
Physical Property
Melting Point
286 °C(lit.)
Safety Information
GHS Signal Word
Warning
European Hazard Symbols
Irritant (Xi)Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Safety Statements
26-36
German water hazard class
3
Risk Statements
36/37/38
GHS Hazard statements
H315-H319-H335
GHS Precautionary statements
P261-P305+P351+P338
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
MSDS Link
Product Information
Purity
≥99%
Linear Formula
CF3SO3Ag
Molecule Details
Packaging
1, 10, 25 g in glass bottle
Application
Gold Catalysts - 21st Century ′Gold Rush′
Yields olefins from secondary phosphates and thiophosphates. Using this reagent the etherification of alcohols with primary alkyl halides can be accomplished under mild conditions.Used to generate cationic rhodium catalysts from chlororhodium complexes for the hydrophosphination of acetylenes. Also employed as a catalyst for the preparation of silyl ethers by hydrosilylation of aldehydes.
1, 10, 25 g in glass bottle
Application
Gold Catalysts - 21st Century ′Gold Rush′
Yields olefins from secondary phosphates and thiophosphates. Using this reagent the etherification of alcohols with primary alkyl halides can be accomplished under mild conditions.Used to generate cationic rhodium catalysts from chlororhodium complexes for the hydrophosphination of acetylenes. Also employed as a catalyst for the preparation of silyl ethers by hydrosilylation of aldehydes.
Molecular Spectra
No Data Available
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References
No Data Available
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