Ejò (II) Trifluoromethanesulfonate CAS 34946-82-2 Mimo>98.0% (Titration) Aworan Ifihan Factory

Ejò (II) Trifluoromethanesulfonate CAS 34946-82-2 Mimọ> 98.0% (Titration) Factory

Apejuwe kukuru:

Orukọ: Ejò (II) Trifluoromethanesulfonate

Synonyms: Ejò (II) Triflate;Ku (OTf)2

CAS: 34946-82-2

Mimọ:> 98.0% (Titration)

Irisi: Pa-White to Light Blue Ri to

E-Mail: alvin@ruifuchem.com

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ọja Tags

Apejuwe:

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

Kemikali Properties:

Orukọ Kemikali	Ejò (II) Trifluoromethanesulfonate
Awọn itumọ ọrọ sisọ	Ejò Trifluoromethanesulfonate;Ejò (II) Triflate;Trifluoromethanesulfonic Acid Ejò (II) Iyọ;Ku (OTf)2
Nọmba CAS	34946-82-2
NỌMBA CAT	RF-PI2078
Iṣura Ipo	Ninu Iṣura, Iwọn iṣelọpọ Ti o to Awọn Toonu
Fọọmu Molecular	C2CuF6O6S2
Òṣuwọn Molikula	361.67
Omi Solubility	Tiotuka ninu Omi
Ifamọ	Hygroscopic
Ojuami Iyo	≥300℃
Ibi ipamọ otutu.	Atmosphere Inert, Yara otutu
Brand	Ruifu Kemikali

Awọn pato:

Nkan	Awọn pato
Ifarahan	Pa-White to Light Blue ri to
Mimọ / Analysis Ọna	> 98.0% (Titration)
Ọrinrin	<0.20%
Erogba nipa Elemental Analysis	6.0 ~ 7.1%
Atẹgun nipasẹ Elemental Analysis	25.5 ~ 26.9%
ICP	Jẹrisi Cu irinše timo
Infurarẹẹdi julọ.Oniranran	Ni ibamu si Eto
Igbeyewo Standard	Standard Enterprise

Package & Ibi ipamọ:

Package:25kg / Ilu, tabi ni ibamu si ibeere alabara

Ipò Ìpamọ́:Fipamọ sinu awọn apoti ti a fi edidi ni itura ati ibi gbigbẹ;Dabobo lati ina ati ọrinrin

Awọn anfani:

FAQ:

Ohun elo:

Ejò (II) Trifluoromethanesulfonate (CAS: 34946-82-2) ni a maa n lo bi ayase fun Mannich condensation, Annulative amination, Friedel-Crafts reaction, Henry reaction, Hypervalent iodine reagent-mediated igbaradi ti carbazoles, Intramolecular oxidative CN bond formation fun awọn kolaginni ti carbazoles, awọn daradara afikun ti trimethylsilyl cyanide to carbonyl agbo.Oruka-Nsii ti epoxides ati aziridines.Àfikún conjugate asymmetric ti organozinc reagents si α, β-unsaturated ketones.Electrophilic afikun ti olefins.Asymmetric aziridination ti olefins.Asymmetric cycloadditions ati aldol condensations.Aibaramu Kharasch ifoyina.Asymmetric Michael afikun ti enamides.Asymmetric OH tabi OR awọn aati ifibọ.Enantioselective intramolecular aminooxygenation ti alkenes.Afikun Enantioselective ti awọn reagents dialkylzinc si iyọ N-acylpyridinium.Pd-catalyzed CH functionalizations of oximes with arylboronic acids.Ti a lo bi Lewis acid ni cyclization Nazarov.Ayase ni diacetoxylation olefins.Ayase ni meta-yan taara arylation ti α-aryl carbonyl agbo.Aṣeyọri ninu idapọ ẹya mẹta ti amines, aldehydes, ati alkynes.