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CAS RN: 2923-28-6 | 产品编码: T1331
Silver Trifluoromethanesulfonate

产品编码 | T1331 |
纯度/分析方法 | >98.0%(T) |
分子式/分子量 | CAgF__3O__3S = 256.93 |
外观与形状(20°C) | 固体 |
储存温度 | 室温 (15°C以下阴凉干燥处) |
储存在惰性气体下 | 存放于惰性气体之中 |
应避免的情况 | 光,空气,湿气 (吸湿) |
包装和容器 | 1G-Glass Bottle with Plastic Insert (查看图片) |
CAS RN | 2923-28-6 |
Reaxys-RN | 3598402 |
PubChem物质ID | 87577100 |
MDL编号 | MFCD00013226 |
技术规格
Appearance | White to Light yellow powder to crystal |
Purity(Precipitation Titration) | min. 98.0 % |
物性(参考值)
水溶性 | 可溶 |
GHS
象形图 |
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信号词 | Warning |
危险性说明 | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
防范说明 | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
相关法规
运输信息
HS编码* | 2843.29-000 |
应用
Methylation of Alcohols using Silver(I) Triflate and Methyl Iodide
Reference
- Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols
- P. G. M. Wuts, in Greene’s Protective Groups in Organic Synthesis, 5th ed., ed. by P. G. M. Wuts, John Wiley & Sons, Inc., Hoboken, New Jersey, 2014, Chap. 2, 17.
应用
AgOTf/CuI–Co-catalyzed Tandem Alkynylation–Cyclization Reaction of N-Iminoisoquinolinium Ylide
Typical procedure (entry 1: R1 = Me, R2 = H, R3 = Ph, R4 = p-MeOC6H4): A mixture of 4-methyl-N'-[5-methyl-2-(phenylethynyl)benzylidene]benzenesulfonohydrazide (77.7 mg, 0.2 mmol) and silver triflate (5.1 mg, 0.02 mmol) in anhydrous 1,2-dichloroethane (0.5 mL) is heated at 70 °C for 1 h. The mixture is then cooled to room temperature. Copper(I) iodide (3.8 mg, 0.02 mmol) and a solution of DBU (91 mg, 0.6 mmol) and 1-(bromoethynyl)-4-methoxybenzene (63.3 mg, 0.3 mmol) dissolved in 1,2-dichloroethane (2 mL) are added subsequently. The mixture is stirred at 70 °C overnight. After the reaction, the solvent is evaporated. The residue is diluted with EtOAc (10 mL), washed with H2O (10 mL), and dried over anhydrous MgSO4. Evaporation of the solvent followed by purification on silica gel column chromatography provides 2-(4-methoxyphenyl)-9-methyl-5-phenylpyrazolo[5,1-a]isoquinoline as a white solid (58.3 mg, yield 80 %).
References
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