Copper(II) Trifluoromethanesulfonate CAS 34946-82-2 Maʻemaʻe >98.0% (Titration) Kiʻi Hōʻike ʻia o ka Hale Hana

Copper(II) Trifluoromethanesulfonate CAS 34946-82-2 Maʻemaʻe >98.0% (Titration) Hale Hana

ʻO ka wehewehe pōkole:

Inoa: Copper(II) Trifluoromethanesulfonate

Synonyms: Copper(II) Triflate;Cu(OTf)2

CAS: 34946-82-2

Maʻemaʻe: >98.0% (Titration)

ʻAno: Keʻokeʻo-keʻokeʻo a i ʻulaʻula Māmā

E-Mail: alvin@ruifuchem.com

E hoʻouna i ka leka uila iā mākou

Huahana Huahana

Nā Huahana Pili

Huahana Huahana

wehewehe:

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

Na Waiwai Kemika:

Inoa Kimia	Copper(II) Trifluoromethanesulfonate
Nā huaʻōlelo like	Copper Trifluoromethanesulfonate;Copper(II) Triflate;Trifluoromethanesulfonic Acid Copper(II) Paakai;Cu(OTf)2
Helu CAS	34946-82-2
Helu CAT	RF-PI2078
Kūlana Kūʻai	Ma ka waihona, hoʻonui ʻia a hiki i nā tona
ʻĀpana Molekala	C2CuF6O6S2
Kaumaha Molecular	361.67
Hiki i ka wai	Hiki i ka wai
ʻO ka ʻike	Hygroscopic
Lae hehee	≥300 ℃
Waihona Temp.	Ka Lewa Inert, Ka Mahana lumi
Brand	Kemika Ruifu

Nā kikoʻī:

'ikamu	Nā kikoʻī
Ka nana aku	Paʻa-keʻokeʻo a ʻulaʻula
Maʻemaʻe / Kaʻina Hanana	>98.0% (Titration)
Mākū	<0.20%
Kalapona ma ka Elemental Analysis	6.0-7.1%
Oxygen by Elemental Analysis	25.5-26.9%
ICP	Hōʻoiaʻiʻo ʻia nā ʻāpana Cu
Infrared Spectrum	Kūlike i ka hoʻolālā
Kūlana hoʻāʻo	Kūlana ʻoihana

Pūʻolo a me ka waiho ʻana:

Pūʻolo:25kg / Drum, a i ʻole e like me ka makemake o ka mea kūʻai aku

Kūlana mālama:E mālama i loko o nā pahu i hoʻopaʻa ʻia ma kahi maloʻo a maloʻo;E pale i ka malamalama a me ka wai

Pono:

FAQ:

Noi:

Hoʻohana mau ʻia ʻo Copper(II) Trifluoromethanesulfonate (CAS: 34946-82-2) ma ke ʻano he catalyst no ka condensation Mannich, Annulative amination, Friedel-Crafts reaction, Henry reaction, Hypervalent iodine reagent-mediated preparation of carbazoles, Intramolecular oxidative CN bond formation for the synthesis o nā carbazoles, ka hoʻohui kūpono o ka trimethylsilyl cyanide i nā pūhui carbonyl.Ke apo-Wehe ana i na epoxides a me aziridines.Asymmetric conjugate hoʻohui o organozinc reagents i α,β-unsaturated ketones.Hoʻohui electrophilic o nā olefins.Asymmetric aziridination o olefins.Asymmetric cycloadditions a me aldol condensations.Asymmetric Kharasch oxidation.Asymmetric Michael hoʻohui o enamides.Asymmetric OH a i ʻole OR hoʻokomo ʻana.Enantioselective intramolecular aminooxygenation o nā alkenes.Hoʻohui Enantioselective o nā reagents dialkylzinc i nā paʻakai N-acylpyridinium.Pd-catalyzed CH functionalizations o oximes me arylboronic acids.Hoʻohana ʻia e like me ka waikawa Lewis i ka cyclization Nazarov.Catalyst i ka diacetoxylation olefins.Catalyst i ka meta-koho pololei arylation o α-aryl carbonyl pūhui.Catalyst i loko o ka hui 'ekolu-hui o na amine, aldehydes, a me alkynes.