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CAS RN: 14353-88-9 | 产品编码: B1616

[Bis(trifluoroacetoxy)iodo]pentafluorobenzene


纯度/分析方法: >97.0%(T)
别名:
  • [双(三氟乙酰氧基)碘代]五氟苯
  • 五氟[双(三氟乙酰氧基)碘]苯
  • Pentafluoro[bis(trifluoroacetoxy)iodo]benzene
  • FPIFA
产品文档:
1G
S$159.00
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5G
S$513.00
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产品编码 B1616
纯度/分析方法 >97.0%(T)
分子式/分子量 C__1__0F__1__1IO__4 = 519.99 
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
包装和容器 1G-Glass Bottle with Plastic Insert (查看图片)
CAS RN 14353-88-9
Reaxys-RN 2030069
PubChem物质ID 87564517
SDBS (AIST Spectral DB) 19381
MDL编号

MFCD00191612

技术规格
Appearance White to Almost white powder to crystal
Purity(Iodometric Titration) min. 97.0 %
Melting point 118.0 to 122.0 °C
物性(参考值)
熔点 120 °C
溶解性(可溶于) 甲醇
GHS
象形图 Pictogram
信号词 Danger
危险性说明 H314 : Causes severe skin burns and eye damage.
防范说明 P501 : Dispose of contents/ container to an approved waste disposal plant.
P260 : Do not breathe dusts or mists.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection.
P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower.
P301 + P330 + P331 : IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P363 : Wash contaminated clothing before reuse.
P304 + P340 + P310 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/doctor.
P305 + P351 + P338 + P310 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/doctor.
P405 : Store locked up.
相关法规
运输信息
UN编号 UN1759
类别 8
包装类别 III
HS编码* 2931.90-000
*此H.S.编码用于日本出口报关,不适用于您所在国家或地区的进口申报
应用
Visible-Light Photoredox Trifluoromethylation via Perfluoroarene Iodine(III) Reagent Decarboxylaytion

Experimental procedure: A Schlenk flask is charged with tris(2,2'-bipyridine)ruthenium(II) bis(hexafluorophosphate) (9.0 mg, 0.01 mmol, 2 mol%), [bis(trifluoroacetoxy)iodo]pentafluorobenzene (650.0 mg, 1.25 mmol, 2.5 equiv.), 2,6-dibromopyridine (0.5 mmol, 1.0 equiv.). Then, acetonitrile (7.5 mL) is added to the reaction mixture. The mixture is degassed twice by the freeze-pump-thaw procedure, then irradiated under blue LED strips (4.8 W). The reaction mixture is subsequently stirred at 35 °C for 12 h. After the reaction is completed, it is diluted with water (8.0 mL). The aqueous phase is extracted with ether (8.0 mL) three times. The combined organic layers are washed with brine and dried over anhydrous sodium sulfate, and are concentrated in vacuo. The residue is purified by silica gel column chromatography (hexane) to afford 2,6-dibromo-3-(trifluoromethyl)pyridine in 32% yield (48.8 mg).

References


应用
Mild Oxidizing Reagent

References


参考文献


产品文档 (部分产品的分析图谱无法提供,敬请谅解。)
化学品安全说明书(SDS)
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技术规格
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