Aeris (II) Trifluoromethanesulfonate CAS 34946-82-2 Puritas > 98.0% (Titration) Factory
Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Copper(II) Trifluoromethanesulfonate (CAS: 34946-82-2) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com
Nomen chemicum | Aeris (II) Trifluoromethanesulfonate |
Synonyma | Aeris Trifluoromethanesulfonate;Copper(II) Triflate;Trifluoromethanesulfonic Acid Copper (II) Salt;Cu(OTf)2 |
CAS Number | 34946-82-2 |
CATTUS Number | RF-PI2078 |
Stock Status | In Stock, Productio Ascendite ad Tons |
Formulae hypotheticae | C2CuF6O6S2 |
M. Pondus | 361.67 |
Aqua Solubility | Solutum in aqua |
Sensibilitas | Hygroscopic |
Liquescens punctum | ≥300℃ |
Repono Nativ. | Inert atmosphaerae, locus Temperature |
Brand | Ruifu Chemical |
Item | Specifications |
Aspectus | Off-White ut caerulei solidi |
Puritas / Analysis Methodus | >98.0% (Titration) |
umor | <0.20% |
Carbon by Elemental Analysis | 6.0~7.1% |
Oxygen by Elemental Analysis | 25.5~26.9% |
ICP | Confirmat Cu Components confirmatus |
Infrared Imaginis | Conformat ut Structure |
Test Standard | Enterprise Standard |
sarcina:25kg / Drum, vel secundum postulationem elit
Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine et humore
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Aeris (II) Trifluoromethanesulfonate (CAS: 34946-82-2) plerumque adhibetur ut catalysta pro condensatione Mannich, aminatio annalitiva, Friedel-Crafts reactionem, Henricum reactionem, praeparationem carbazolorum hypervalent iodi reo-mediatae, intramoleculares oxidative CN formatio vinculi. synthesis carbazolorum, efficientis adiectio trimethylsilyl cyanidi ad compositorum carbonylorum.Ring-Openatio epoxidum et aziridinum.Asymmetrica coniugata additionis organozinc reagentium ad α, β ketones unsaturated.Additio electronica olefins.Aziridinatio olefins asymmetrica.Cycloadditiones asymmetricae et condensationes aldol.Oxidatio asymmetrica Kharasch.Asymmetrica Michaelis additamenta enamides.Asymmetrica OH vel OR insertio profectae.Aminooxygenatum alkenum enantioselectivum intramolecularis.Enantioselectivae additionis dialkylzinci reagentia ad N-acylpyridinium salium.Pd-catalyzed CH functiones oximentorum cum acida arylboronica.Usus est sicut acidum Lewis in cyclizatione Nazarov.Catalyst in diacetoxylatione olefins.Catalyst in meta-selectiva directa arylatione α carbonyl compositarum.Catalysmus in tribus copulationibus aminibus, aldehydis, et alkynis.
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