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CAS RN: 1045822-31-8 | Product Number: M2782
N-Methyl-N-[(trifluoromethyl)thio]-p-toluenesulfonamide
Purity: >98.0%(GC)(N)
Synonyms:
Product Documents:
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Product Number | M2782 |
Purity / Analysis Method | >98.0%(GC)(N) |
Molecular Formula / Molecular Weight | C__9H__1__0F__3NO__2S__2 = 285.30 |
Physical State (20 deg.C) | Liquid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 1045822-31-8 |
Reaxys Registry Number | 27199071 |
PubChem Substance ID | 354335700 |
Specifications
Purity(GC) | min. 98.0 % |
Purity(with Total Nitrogen) | min. 98.0 % |
NMR | confirm to structure |
Properties (reference)
Flash point | 120 °C |
Refractive Index | 1.50 |
GHS
Related Laws:
Transport Information:
H.S.code* | 2935.90-000 |
Application
Sulfonamide for Nucleophilic and Electrophilic Trifluoromethylthiolations
Experimental procedure2): To a flask are added the boronic acid (0.50 mmol, 1.0 eq.), 4,4'-dimethyl-2,2'-bipyridyl (0.10 mmol, 20 mol%), CuI (0.05 mmol, 10 mol%), diglyme (1.5 mL), N-methyl-N-[(trifluoromethyl)thio]-p-toluenesulfonamide (0.60 mmol, 1.2 eq.) and finally distilled water (3.50 mmol, 7.0 eq.). The reaction mixture is stirred for 15 h at room temperature. The reaction is partitioned between pentane and water. The aqueous layer is extracted with pentane and the combined organic layers are washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The crude residue is purified by flash chromatography to afford the desired product.
References
- 1) Electrophilic Trifluoromethylthiolation of Carbonyl Compounds
- 2) Mild and Soft Catalyzed Trifluoromethylthiolation of Boronic Acids: The Crucial Role of Water
- 3) Metal-Free Direct Nucleophilic Perfluoroalkylthiolation with Perfluoroalkanesulfenamides
PubMed Literature
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[Product Highlights] Sulfonamide for Nucleophilic and Electrophilic TrifluoromethylthiolationsProduct Documents (Note: Some products will not have analytical charts available.)
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