Aeris (II) Trifluoromethanesulfonate CAS 34946-82-2 Puritas > 98.0% (Titration) Factory

Description:

Nomen: Copper (II) Trifluoromethanesulfonate

Synonyma: Copperum (II) Trifolium;Cu(OTf)2

CAS: 34946-82-2

Puritas: >98.0% (Titration)

Aspectus: Off-White ad caeruleum solidum

E-Mail: alvin@ruifuchem.com

Mitte ad nos inscriptio

Product Detail

Product Tags

Descriptio:

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:

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

Specifications:

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 & Repono:

sarcina:25kg / Drum, vel secundum postulationem elit

Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine et humore

commoda:

FAQ:

Applicatio:

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.