Silver trifluoromethanesulfonate 

1, 10, 25 g in glass btl

Yields olefins from secondary phosphates and thiophosphates.¹ Using this reagent the etherification of alcohols with primary alkyl halides can be accomplished under mild conditions.²
Used to generate cationic rhodium catalysts from chlororhodium complexes for the hydrophosphination of acetylenes.³ Also employed as a catalyst for the preparation of silyl ethers by hydrosilylation of aldehydes.⁴

≥99%

286 °C(lit.)

1. Tet. Lett. 36, 719, (1995)

2. Tet. Lett. 35, 8111, (1994)

3. J. Org. Chem. 71, 9248, (2006) abstract

4. Chem. Commun. , 1359, (2006)

Beil. 3,IV,34

Fieser 6,520 / Fieser 7,324 / Fieser 9,414 / Fieser 12,435 / Fieser 13,274 / Fieser 14,282 / Fieser 16,302 / Fieser 17,314

Aldrich MSDS 1, 1604:D / Corp MSDS 1 (2), 3099:C / FT-IR 2 (1), 1506:C / FT-IR 1 (2), 1231:C / IR-Spectra (3), 533:E / RegBook 1 (1), 1055:L / Sigma FT-IR 1 (2), 947:D / Structure Index 1, 163:B:9

3