Mhangura(II) Trifluoromethanesulfonate CAS 34946-82-2 Kuchena > 98.0% (Titration) Factory

Tsanangudzo Pfupi

Zita: Mhangura(II) Trifluoromethanesulfonate

Anoreva zvakafanana: Mhangura(II) Triflate;Cu(OTf)2

CAS: 34946-82-2

Kuchena:> 98.0% (Titration)

Chitarisiko: Off-White kune Chiedza cheBlue Solid

E-Mail: alvin@ruifuchem.com

Tumira email kwatiri

Product Detail

Product Tags

Tsanangudzo:

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

Chemical Properties:

Chemical Name	Mhangura (II) Trifluoromethanesulfonate
Mashoko anoreva zvakafanana	Copper Trifluoromethanesulfonate;Mhangura(II) Triflate;Trifluoromethanesulfonic Acid Copper(II) Munyu;Cu(OTf)2
Nhamba yeCAS	34946-82-2
Nhamba yeCAT	RF-PI2078
Stock Status	MuStock, Kugadzirwa Kunokwira Kusvika Matani
Molecular Formula	C2CuF6O6S2
Molecular Weight	361.67
Mvura Solubility	Soluble mumvura
Sensitivity	Hygroscopic
Melting Point	≥300℃
Storage Temp.	Inert Atmosphere, Kamuri Tembiricha
Brand	Ruifu Chemical

Zvinotsanangurwa:

Item	Zvinotsanangurwa
Chitarisiko	Off-White kune Chiedza cheBlue Solid
Kuchena / Analysis Method	>98.0% (Titration)
Unyoro	<0.20%
Carbon neElemental Analysis	6.0~7.1%
Okisijeni neElemental Analysis	25.5 ~ 26.9%
ICP	Inosimbisa Cu Zvikamu Zvakasimbiswa
Infrared Spectrum	Inopindirana neChimiro
Test Standard	Enterprise Standard

Package & Kuchengeta:

Package:25kg / Drum, kana zvinoenderana nezvinodiwa nemutengi

Storage Condition:Chengetedza mumidziyo yakavharwa panzvimbo inotonhorera uye yakaoma;Dzivirira kubva kuchiedza uye unyoro

Zvakanakira:

FAQ:

Application:

Mhangura (II) Trifluoromethanesulfonate (CAS: 34946-82-2) inowanzoshandiswa se catalyst yeMannich condensation, Anulative amination, Friedel-Crafts reaction, Henry reaction, Hypervalent iodine reagent-mediated kugadzirira kwe carbazoles, Intramolecular oxidative CN bond formation. synthesis ye carbazoles, iyo inobudirira yekuwedzera ye trimethylsilyl cyanide kune carbonyl makomisheni.Mhete-Kuvhurwa kwe epoxides uye aziridines.Asymmetric conjugate kuwedzerwa kweorganozinc reagents kune α, β-unsaturated ketones.Electrophilic kuwedzera kweolefins.Asymmetric aziridination yeolefins.Asymmetric cycloadditions uye aldol condensations.Asymmetric Kharasch oxidation.Asymmetric Michael kuwedzera kwe enamides.Asymmetric OH kana OR kuisa maitiro.Enantioselective intramolecular aminooxygenation yealkenes.Enantioselective kuwedzera kwedialkylzinc reagents kuN-acylpyridinium munyu.Pd-catalyzed CH functionalizations yeoximes ine arylboronic acids.Inoshandiswa se Lewis acid muNazarov cyclization.Catalyst mu diacetoxylation olefins.Catalyst mune meta-selective yakananga arylation ye-α-aryl carbonyl makomisheni.Catalyst mukubatana kwezvikamu zvitatu zveamines, aldehydes, uye alkynes.