トリフルオロメタンスルホン酸銅(II)(34946-82-2)

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トリフルオロメタンスルホン酸銅(II) 製品概要
化学名:トリフルオロメタンスルホン酸銅(II)
英語化学名:COPPER(II) TRIFLUOROMETHANESULFONATE
别名:Copper (Ii) Trifluorome;Copper(II) trifluoromethanesulfonate,Copper(II) triflate, Cupric trifluoromethanesulfonate, Trifluoromethanesulfonic acid copper(II) salt;Copper(II) trifluoromethanesulfonate 98%;Trifluoromethanesulfonic acid copper(II);Copper(Ⅱ) trifluoroMethanesulfonate;Cupric trifluoroMethylsulfonate;Copper(II) trifluoroMethanesulfonate,98% Cu(CF3SO3)2;Copper(II) Triflate Trifluoromethanesulfonic Acid Copper(II) Salt
CAS番号:34946-82-2
分子式:C2CuF6O6S2
分子量:361.68
EINECS:252-300-8
カテゴリ情報:Biochemistry;Catalysts for Organic Synthesis;Classes of Metal Compounds;Cu (Copper) Compounds;Homogeneous Catalysts;Metal Triflates;Reagents for Oligosaccharide Synthesis;Synthetic Organic Chemistry;Transition Metal Compounds;Cu;OTf&NTf series;triflate;metal triflate compounds
Mol File:34946-82-2.mol
トリフルオロメタンスルホン酸銅(II)
トリフルオロメタンスルホン酸銅(II) 物理性質
融点 ≥300 °C
貯蔵温度 Inert atmosphere,Room Temperature
溶解性Water (Slightly)
外見 Powder
White to slightly blue or light gray
水溶解度 Soluble in water.
Sensitive Hygroscopic
Hydrolytic Sensitivity6: forms irreversible hydrate
BRN 4028198
暴露限界値ACGIH: TWA 1 mg/m3
NIOSH: IDLH 100 mg/m3; TWA 1 mg/m3
安定性:hygroscopic
InChIKeySBTSVTLGWRLWOD-UHFFFAOYSA-L
CAS データベース34946-82-2(CAS DataBase Reference)
安全性情報
主な危険性 C,Xi
Rフレーズ 34
Sフレーズ 26-36/37/39-45-27
RIDADR UN 3261 8/PG 2
WGK Germany 3
3-10
Hazard Note Irritant/Hygroscopic
TSCA No
国連危険物分類 8
容器等級 III
HSコード 29049085
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
トリフルオロメタンスルホン酸銅(II) Usage And Synthesis
外観白色〜うすい青色又は灰色, 結晶性粉末〜粉末又は塊
溶解性水に溶ける。
用途試験研究用。
使用上の注意アルゴン封入
化学的特性white to slightly blue or light grey cryst. powder
使用Copper(II) trifluoromethanesulfonate is a mild lewis acid. It is used as catalyst which promotes dehydration of alcohols and diols to alkenes at ambient temperatures. It is widely used to generate carbenoid species from ?-diazo esters and ketones, via in situ reduction to the Cu(I) species. It is also promotes the reaction between diazo esters and imines to give aziridines. It catalyzes syn-selective aldol condensation of (Z)-silyl enol ethers with aldehydes, Friedel-Crafts alkylation, acylation reactions of aromatics and addition of trimethylsilyl cyanide to carbonyl compounds.
純化方法Dissolve it in MeCN, add dry Et2O until cloudy and cool at -20o in a freezer. The light blue precipitate is collected and dried in a vacuum oven at 130o/20mm for 8hours. It has 737nm ( 22.4 max M1cm -1) in AcOH. [Salomon & Kochi J Am Chem Soc 95 330 1973]. It has also been dried in a vessel at 0.1Torr by heating with a Fischer burner [Andrist et al. J Org Chem 43 3422 1978]. It has been dried at 110-120o/5mm for 1hour before use and forms a *benzene complex which should be handled in a dry box because it is air sensitive [Kobayashi et al. Chem Pharm Bull Jpn 28 262 1980, Salomon & Kochi J Am Chem Soc 95 330 1973]. [Beilstein 3 IV 34.]
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