Rhodium(II) Acetate Dimer CAS 15956-28-2 Rh 43.0~46.6%

Tlhaloso e Khutšoanyane:

Lebitso la Lik'hemik'hale: Rhodium (II) Acetate Dimer

CAS: 15956-28-2

Rh: 46.5%

Bohloeki: ≥99.95% Metals Basics

Ponahalo: Phofo e tala

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Lintho tsa Lik'hemik'hale:

Lebitso la Lik'hemik'hale	Rhodium (II) Acetate Dimer
Litlhaloso tse tšoanang	Dirhodium(II) Tetraacetate;Tetrakis(acetato)dirhodium(II);Tetrakis[micron-(acetato-O:O')]dirhodium;Tetrakis(μ-acetato)di-rhodium (Rh-Rh);Tetrakis[μ-(acetato-O:O')]di-Rhodium(Rh-Rh)
Nomoro ea CAS	15956-28-2
Nomoro ea KAtse	RF2727
Boemo ba Setoko	Ka Setokong, Sekhahla sa Tlhahiso Ho fihlela ho Lithane
Foromo ea limolek'hule	C8H12O8Rh2
Boima ba Molek'hule	441.99
Melting Point	205 ℃
Botenya	1.126 g/cm3
Botsitso	Hygroscopic
Solubility	E qhibiliha ka Tharollo ea Aqueous Joalo ka Metsi.E qhibiliha hanyenyane ka Ethanol
Brand	Ruifu Chemical

Litlhaloso:

Ntho	Litlhaloso
Ponahalo	Phofo e tala
Rh (Analysis ea Gravimetric)	43.0~46.6%
ICP	E netefatsa Karolo ea Rhodium e Tiisitsoe
Infrared Spectrum	E Ikamahanya le Sebopeho
Phapang ea X-Ray	E Ikamahanya le Sebopeho
Tekanyetso ea Teko	Maemo a Khoebo

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Kopo:

Rhodium (II) Acetate Dimer (CAS: 15956-28-2), CH Bond Activation Reaction, Transition Metal Catalysts, Binuclear Rhodium Complexes e Atlehang bakeng sa Foromo e Nyenyane le e Mehareng.Rhodium(II) Acetate Dimer ke mohloli o atlehang oa ho etsa li-ylide hape ke mohloli oa cyclopropanation ea alkenes, oxidation ea joala, liketso tsa cyclization tse kenyelletsang -diazo carbonyl lihlopha, ho kenngoa ka CH le XH bond (XH ke NH kapa SH kapa OH) .E sebetsa haholoanyane hape e thusa ho khetholla li-ribonucleosides le deoxynucleosides.E boetse e sebelisoa ho etsa hore fullerenes e sebetse ka li-polymers.Mokhoa o sebetsang oa ho fetisa hydrogen ho tloha 2-propanol ho ea cyclohexanone le metsoako e meng e sa tsitsang.Catalyst bakeng sa ho kenngoa ka har'a li-bond tsa CH le XH.Catalyst bakeng sa moloko oa Ylide.Karabelo ea Doyle Kirmse ea Allylic Sulfides le Diazoalkane.Claisen rearrangement.Li-epoxide tse tsoang ho aldehydes.Synthesis ea aziridines ho tsoa ho allylic N-tosyloxycarbamates.Rh / NHC e ile ea kenya letsoho ka ho toba intermolecular arylation ea CH bonds.Chiral Bronsted acid-Rh e ile ea susumetsa likarolo tse tharo tsa metsoako ea diazo ka joala le imines.Rh-catalyzed cyclopropenations ea ynamides.Tandem asymmetric aza-Darzens/mesebetsi ea ho bula lesale.