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| | INDIUM(III) TRIFLUOROMETHANESULFONATE Basic information |
| | INDIUM(III) TRIFLUOROMETHANESULFONATE Chemical Properties |
| Melting point | >300°C | | storage temp. | Inert atmosphere,Room Temperature | | solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | | form | Powder and Granules | | color | Off-white | | Water Solubility | Slightly soluble in hydrocarbons and diethyl ether. Insoluble in water | | Sensitive | Hygroscopic | | Stability: | hygroscopic | | InChIKey | UCYRAEIHXSVXPV-UHFFFAOYSA-K | | CAS DataBase Reference | 128008-30-0(CAS DataBase Reference) |
| Hazard Codes | Xi,C | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | RIDADR | UN3261 | | WGK Germany | 3 | | F | 3-10 | | Hazard Note | Corrosive/Hygroscopic | | HazardClass | 8 | | PackingGroup | II | | HS Code | 29310099 |
| | INDIUM(III) TRIFLUOROMETHANESULFONATE Usage And Synthesis |
| Chemical Properties | Off-white powder and granules | | Uses | Reactant or reagent involved in:
- Synthesis of stable indium bacteriochlorins
- Studying basicities of phosphoryl compounds toward triflates Lewis acids
- Preparation of decahydroquinoline-type toxins via intramolecular hetero Diels-Alder reactions
Catalyst for synthesis of benzoxazoles via cyclocondensations | | Uses | Indium(III) trifluoromethanesulfonate is used as a Lewis acid catalyst in organic synthesis and as a co-catalyst in organometallic catalysis. It is also used as a reactant in the preparation of stable indium bacteriochlorins and decahydroquinoline-type toxins through intramolecular hetero Diels-Alder reactions. Further, it is used in the synthesis of benzoxazoles through cyclocondensations. | | reaction suitability | core: indium
reagent type: catalyst |
| | INDIUM(III) TRIFLUOROMETHANESULFONATE Preparation Products And Raw materials |
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