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Type | HazMat fee for 500 gram (Estimated) |
Excepted Quantity | USD 0.00 |
Limited Quantity | USD 15-60 |
Inaccessible (Haz class 6.1), Domestic | USD 80+ |
Inaccessible (Haz class 6.1), International | USD 150+ |
Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |
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* Storage: {[proInfo.prStorage]}
CAS No. : | 1640084-14-5 | MDL No. : | MFCD30187371 |
Formula : | C10H11F3OS | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | VYAJORZDVDXTAC-UHFFFAOYSA-N |
M.W : | 236.25 | Pubchem ID : | 121540554 |
Synonyms : |
|
Signal Word: | Danger | Class: | 8,3 |
Precautionary Statements: | P501-P240-P210-P233-P243-P241-P242-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P403+P235 | UN#: | 2920 |
Hazard Statements: | H314-H226 | Packing Group: | Ⅱ |
GHS Pictogram: |
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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
87% | With triethylamine In dichloromethane at 20℃; for 0.0833333h; | |
87% | With triethylamine In dichloromethane at 20℃; for 0.0833333h; | 18 Example 18 50mL egg-shaped flask was added N - saccharin trifluoromethylthio group 1 (184mg, 0.65mmol), 2- methyl-2-phenylethanol (69.0mg, 0.5mmol), 160μL (1.15mmol) of triethylamine, dichlorobis methane (10 mL), at room temperature for 5min.After completion of the reaction, the reaction solution rapidly by about 6 millimeters silica gel column, the column with the amount of methylene chloride and washed twice, and the combined organic liquid, spin dry to give trifluoromethyl - (2-phenyl) isopropyl thio peroxide (103mg, 87% isolated yield).Purity by NMR identified more than 95%.Trifluoromethyl - (2-phenyl) peroxy isopropyl-thio (((2-phenylpropan-2-YL) Oxy) (trifluoromethyl) sulfane): |
80% | With triethylamine In dichloromethane at 20℃; for 0.0833333h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
81% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
75% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
61% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
62% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
70% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
75% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
79% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
79% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
77% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
75% | With Iron(III) nitrate nonahydrate; borane-THF In water; acetonitrile at 0℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
60% | With [2,2]bipyridinyl; copper(I) thiophene-2-carboxylate; potassium carbonate In toluene at 120℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
49% | Stage #1: 1-Phenyl-2-propen-1-ol With dmap In dichloromethane at 20℃; for 0.5h; Inert atmosphere; Stage #2: (((2-phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane) In dichloromethane at 20℃; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | With [2,2]bipyridinyl; tetrakis(actonitrile)copper(I) hexafluorophosphate; potassium carbonate In diethylene glycol dimethyl ether at 35℃; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | With [2,2]bipyridinyl; tetrakis(actonitrile)copper(I) hexafluorophosphate; potassium carbonate In diethylene glycol dimethyl ether at 35℃; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
68% | With [2,2]bipyridinyl; copper(I) bromide dimethylsulfide complex; potassium carbonate In 1,2-dichloro-ethane at 80℃; for 14h; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
66% | With [2,2]bipyridinyl; copper(I) bromide dimethylsulfide complex; potassium carbonate In 1,2-dichloro-ethane at 80℃; for 14h; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
70% | With [2,2]bipyridinyl; copper(I) bromide dimethylsulfide complex; potassium carbonate In 1,2-dichloro-ethane at 80℃; for 14h; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
86% | With [2,2]bipyridinyl; copper(I) bromide dimethylsulfide complex; potassium carbonate In 1,2-dichloro-ethane at 80℃; for 14h; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
92% | With [2,2]bipyridinyl; copper(I) bromide dimethylsulfide complex; potassium carbonate In 1,2-dichloro-ethane at 80℃; for 14h; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
72% | With [2,2]bipyridinyl; copper(I) bromide dimethylsulfide complex; potassium carbonate In 1,2-dichloro-ethane at 80℃; for 14h; Schlenk technique; Inert atmosphere; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
69% | With camphor-10-sulfonic acid In 1,2-dichloro-ethane at 40℃; for 48h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | With camphor-10-sulfonic acid In 1,2-dichloro-ethane at 40℃; for 48h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
94% | With camphor-10-sulfonic acid In 1,2-dichloro-ethane at 40℃; for 48h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
91% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
75% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
81% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
91% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | With dmap In dichloromethane at 20℃; for 12h; Schlenk technique; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
71% | With dilauryl peroxide In chlorobenzene at 100℃; for 4h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | With triethylamine In dichloromethane at 20℃; for 0.0833333h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
97% | With [(1,2-bis(diphenylphosphino)ethane)CuCl]; sodium t-butanolate In toluene at 50℃; for 2h; Inert atmosphere; Schlenk technique; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
86% | With [(1,2-bis(diphenylphosphino)ethane)CuCl]; sodium t-butanolate In toluene at 50℃; for 2h; Inert atmosphere; Schlenk technique; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
96% | With [(1,2-bis(diphenylphosphino)ethane)CuCl]; sodium t-butanolate In toluene at 50℃; for 2h; Inert atmosphere; Schlenk technique; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
72% | With [(1,2-bis(diphenylphosphino)ethane)CuCl]; sodium t-butanolate In toluene at 50℃; for 2h; Inert atmosphere; Schlenk technique; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
94% | With [(1,2-bis(diphenylphosphino)ethane)CuCl]; sodium t-butanolate In toluene at 50℃; for 2h; Inert atmosphere; Schlenk technique; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
92% | With [(1,2-bis(diphenylphosphino)ethane)CuCl]; sodium t-butanolate In toluene at 50℃; for 12h; Inert atmosphere; Schlenk technique; |