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Scandium(III) triflate - 98%, high purity , CAS No.144026-79-9

  • ≥98%
Item Number
S106648
Grouped product items
SKUSizeAvailabilityPrice Qty
S106648-250mg
250mg
In stock
$21.90
S106648-1g
1g
In stock
$51.90
S106648-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$157.90
S106648-10g
10g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$249.90
S106648-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$499.90
S106648-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,199.90

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.

Basic Description

Synonyms144026-79-9|Scandium(III) trifluoromethanesulfonate|Scandium trifluoromethanesulfonate|Scandium(III) triflate|Scandium Triflate|SC(OTF)3|MFCD00192433|scandium(3+);trifluoromethanesulfonate|scandium(III)trifluoromethanesulfonate|Trifluoromethanesulfonic ac
Specifications & Purity98%
Storage TempArgon charged
Shipped InNormal
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.

Names and Identifiers

IUPAC Name scandium(3+);trifluoromethanesulfonate
INCHI InChI=1S/3CHF3O3S.Sc/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
InChi Key HZXJVDYQRYYYOR-UHFFFAOYSA-K
Canonical SMILES C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[Sc+3]
Isomeric SMILES C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[Sc+3]
WGK Germany 3
PubChem CID 2734571
UN Number 1759
Molecular Weight 492.16
Beilstein 8510151
Reaxy-Rn 8510151

Certificates

Certificate of Analysis(COA)

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28 results found

Lot NumberCertificate TypeDateItem
F2426229Certificate of AnalysisJun 15, 2024 S106648
F2426227Certificate of AnalysisJun 15, 2024 S106648
F2426092Certificate of AnalysisJun 15, 2024 S106648
F2426091Certificate of AnalysisJun 15, 2024 S106648
F2426090Certificate of AnalysisJun 15, 2024 S106648
H2402374Certificate of AnalysisJun 13, 2024 S106648
G2429135Certificate of AnalysisJun 13, 2024 S106648
H2401505Certificate of AnalysisJun 13, 2024 S106648
A2426485Certificate of AnalysisJan 15, 2024 S106648
E2414021Certificate of AnalysisJan 15, 2024 S106648
A2426497Certificate of AnalysisJan 15, 2024 S106648
A2426495Certificate of AnalysisJan 15, 2024 S106648
A2426492Certificate of AnalysisJan 15, 2024 S106648
A2426491Certificate of AnalysisJan 15, 2024 S106648
A2426489Certificate of AnalysisJan 15, 2024 S106648
A2426488Certificate of AnalysisJan 15, 2024 S106648
A2426484Certificate of AnalysisJan 15, 2024 S106648
L1824091Certificate of AnalysisOct 18, 2022 S106648
L2326081Certificate of AnalysisMar 24, 2022 S106648
F2208063Certificate of AnalysisMar 24, 2022 S106648
K2310025Certificate of AnalysisMar 24, 2022 S106648
K2221178Certificate of AnalysisMar 24, 2022 S106648
J2317123Certificate of AnalysisMar 24, 2022 S106648
H2304169Certificate of AnalysisMar 24, 2022 S106648
F2208071Certificate of AnalysisMar 24, 2022 S106648
F2208066Certificate of AnalysisMar 24, 2022 S106648
F2208065Certificate of AnalysisMar 24, 2022 S106648
F2208064Certificate of AnalysisMar 24, 2022 S106648

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Chemical and Physical Properties

SolubilitySoluble in water, alcohol and acetonitrile.
SensitivityHygroscopic.
Melt Point(°C)>300°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
Reaxy-Rn 8510151

Related Documents

Alternative Products

References

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]

Solution Calculators