Copper(II) Trifluoromethanesulfonate CAS 34946-82-2 Purity >98.0% (Titration) Factory

Tlhaloso e Khutšoanyane:

Lebitso: Koporo(II) Trifluoromethanesulfonate

Mantsoe a tšoanang: Koporo(II) Triflate;Cu(OTf)2

CAS: 34946-82-2

Bohloeki: >98.0% (Titration)

Ponahalo: Bosoeu bo Bosoeu ho ea ho Botala bo Botala bo Tiileng

E-Mail: alvin@ruifuchem.com


Lintlha tsa Sehlahisoa

Lihlahisoa tse Amanang

Li-tag tsa Sehlahisoa

Tlhaloso:

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

Lintho tsa Lik'hemik'hale:

Lebitso la Lik'hemik'hale Koporo(II) Trifluoromethanesulfonate
Litlhaloso tse tšoanang Copper Trifluoromethanesulfonate;Koporo(II) Triflate;Trifluoromethanesulfonic Acid Koporo(II) Letsoai;Cu(OTf)2
Nomoro ea CAS 34946-82-2
Nomoro ea KAtse RF-PI2078
Boemo ba Setoko Ka Setokong, Sekhahla sa Tlhahiso Ho fihlela ho Lithane
Foromo ea limolek'hule C2CuF6O6S2
Boima ba Molek'hule 361.67
Ho qhibiliha ha Metsi E qhibilihang ka Metsing
Kutloisiso Hygroscopic
Melting Point ≥300 ℃
Mocheso oa polokelo. Sepakapaka se Senyehileng, Mocheso oa Kamore
Brand Ruifu Chemical

Litlhaloso:

Ntho Litlhaloso
Ponahalo E Tletseng Bosoeu ho isa Boputsoa bo Khanyang
Mokhoa oa Bohloeki / Analysis >98.0% (Titration)
Mongobo <0.20%
Carbon ka Elemental Analysis 6.0~7.1%
Oksijene ka Tlhahlobo ea Elemental 25.5 ~ 26.9%
ICP E netefatsa Likarolo tsa Cu li Tiisitsoe
Infrared Spectrum E Ikamahanya le Sebopeho
Tekanyetso ea Teko Maemo a Khoebo

Sephutheloana le Bobolokelo:

Sephutheloana:25kg/Drum, kapa ho ya ka tlhokahalo ya moreki

Boemo ba polokelo:Boloka ka lijaneng tse koetsoeng sebakeng se phodileng le se omileng;Sireletsa leseli le mongobo

Melemo:

1

LBH:

Kopo:

Copper(II) Trifluoromethanesulfonate (CAS: 34946-82-2) hangata e sebelisoa e le catalyst bakeng sa Mannich condensation, Annulative amination, Friedel-Crafts reaction, Henry reaction, Hypervalent iodine reagent-mediated preparation of carbazoles, Intramolecular oxidative CN bond formation. synthesis ea carbazoles, tlatsetso e sebetsang ea trimethylsilyl cyanide ho metsoako ea carbonyl.Ring-Ho buloa ha epoxides le aziridines.Asymmetric conjugate tlatsetso ea li-reagents tsa organozinc ho α, β-unsaturated ketones.Keketso ea elektrophil ea olefin.Asymmetric aziridination ea olefin.Asymmetric cycloadditions le aldol condensations.Asymmetric Kharasch oxidation.Asymmetric Michael tlatsetso ea enamides.Asymmetric OH kapa OR karabelo ea ho kenya.Enantioselective intramolecular aminooxygenation ea alkenes.Ho eketsoa ha Enantioselective ea li-reagents tsa dialkylzinc ho letsoai la N-acylpyridinium.Pd-catalyzed CH functionalizations ea oximes e nang le arylboronic acid.E sebelisoa e le asiti ea Lewis ho cyclization ea Nazarov.Catalyst ho diacetoxylation olefin.Catalyst ho meta-selective direct arylation ea α-aryl carbonyl metsoako.E thusa ho kopanya likarolo tse tharo tsa li-amine, aldehydes le alkynes.

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