Discover Scandium(III) triflate by Aladdin Scientific in 98% for only $21.90. Available - in Ligands at Aladdin Scientific. Tags: Element classified compounds, Scandiu, Stable Lewis Acids in Aqueous Media, Transition metal compounds, Trifluoromethanesulfonate.
144026-79-9|Scandium(III) trifluoromethanesulfonate|Scandium trifluoromethanesulfonate|Scandium(III) triflate|Scandium Triflate|SC(OTF)3|MFCD00192433|scandium(3+);trifluoromethanesulfonate|scandium(III)trifluoromethanesulfonate|Trifluoromethanesulfonic ac
Specifications & Purity
98%
Storage Temp
Argon charged
Shipped In
Normal
Product Description
Scandium(III) triflate is an important catalyst for Friedel-Crafts acylation, Diels-Alder reactions and other carbon-carbon bond-forming reactions. It also stereochemically catalyzes the radical polymerization of acrylates.Scandium(III) triflate complex of (4′S,5′S)-2,6-bis[4′-(triisopropylsilyl)oxymethyl-5′-phenyl-1′,3′-oxazolin-2′-yl]pyridine has been employed as catalyst for the asymmetric Friedel-Crafts reaction between substituted indoles and methyl (E)-2-oxo-4-aryl-3-butenoates. Scandium(III) triflate was used as catalyst in the following studies: . Hydrothiolation reaction of aromatic and aliphatic thiols. . Selective two-electron reduction of O2 by ferrocene derivatives. . Vinylogous Friedel-Crafts alkylation of indoles and pyrroles in water. . Synthesis of β-cyanoketones. It was also used with triethylsilane to reductively open functionalized pyranoside rings and in the key step of synthesis of bullvalone via a stabilized sulfur ylide.
1.Samikannu Ramesh,Appaswami Lalitha. (2013-10-31) Scandium(III) triflate catalyzed 1,4-addition of cyano group to enones using tetraethylammonium cyanide as the cyanide source.. Acta chimica Slovenica, 60 ((3)):(689-694). [PMID:24169725]
2.Saya Kakuda,Clarence J Rolle,Kei Ohkubo,Maxime A Siegler,Kenneth D Karlin,Shunichi Fukuzumi. (2015-02-11) Lewis acid-induced change from four- to two-electron reduction of dioxygen catalyzed by copper complexes using scandium triflate.. Journal of the American Chemical Society, 137 ((9)):(3330-3337). [PMID:25659416]
3.Krzysztof Kuciński,Piotr Pawluć,Bogdan Marciniec,Grzegorz Hreczycho. (2015-02-18) Highly selective hydrothiolation of unsaturated organosilicon compounds catalyzed by scandium(III) triflate.. Chemistry (Weinheim an der Bergstrasse, Germany), 21 ((13)):(4940-4943). [PMID:25689836]
4.Cholho Choe, Ling Yang, Zhanao Lv, Wanling Mo, Zhuqi Chen, Guangxin Li, Guochuan Yin,. (2015-04-24) Redox-inactive metal ions promoted the catalytic reactivity of non-heme manganese complexes towards oxygen atom transfer.. Dalton transactions (Cambridge, England : 2003), 44 ((19)):( 9182-9192 ). [PMID:25904197]
5.Alec Lutzke,Alyssa C Melvin,Megan J Neufeld,Christopher L Allison,Melissa M Reynolds. (2019-01-11) Nitric oxide generation from S-nitrosoglutathione: New activity of indium and a survey of metal ion effects.. Nitric oxide : biology and chemistry, 84 (16-21). [PMID:30630054]
6.Kazuaki Ishihara,Manabu Kubota,Hideki Kurihara,Hisashi Yamamoto. (1996-07-12) Scandium Trifluoromethanesulfonate as an Extremely Active Lewis Acid Catalyst in Acylation of Alcohols with Acid Anhydrides and Mixed Anhydrides.. The Journal of organic chemistry, 61 ((14)):(4560-4567). [PMID:11667380]
7.Alex R Lippert,Juthanat Kaeobamrung,Jeffrey W Bode. (2006-11-16) Synthesis of oligosubstituted bullvalones: shapeshifting molecules under basic conditions.. Journal of the American Chemical Society, 128 ((46)):(14738-14739). [PMID:17105247]
8.Hua-Li Qin,Jason T Lowe,James S Panek. (2007-01-04) Mild reductive opening of aryl pyranosides promoted by scandium(III) triflate.. Journal of the American Chemical Society, 129 ((1)):(38-39). [PMID:17199277]
9.Giovanni Desimoni,Giuseppe Faita,Marco Toscanini,Massimo Boiocchi. (2008-02-29) Asymmetric Friedel-Crafts alkylation of indoles with methyl (E)-2-oxo-4-aryl-3-butenoates catalyzed by Sc(OTf)3/pybox.. Chemistry (Weinheim an der Bergstrasse, Germany), 14 ((12)):(3630-3636). [PMID:18306268]
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