As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryItems Standard Result Appearance Grass green powder Complies Purity, not less than 99.90
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inquirygood Appearance:White or off white powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:good Transportation:According to the demand of customer Port:shanghai
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inquiryProduct Name: Rhodium(II) octanoate dimer Synonyms: RHODIUM(III)OCTANOATE DIMER;RHODIUM (II) OCTANOATE DIMER;RHODIUM OCTANOATE DIMER;Rhodiumoctanoatedimergreenpowder;Rhodium(II)octanoatedimer,98%;Rhodium(II
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inquiryProduct Name: Rhodium(II) octanoate dimer Synonyms: RHODIUM(III)OCTANOATE DIMER;RHODIUM (II) OCTANOATE DIMER;RHODIUM OCTANOATE DIMER;Rhodium(II)octanoatedimer,98%;Rhodiumoctanoatedimergreenpowder;Rh26%Dirhodium tetraoctanoate;Dirhodium tetraoct
About Product Details Items Specifications Test Results Appearance White to white crystalline powde
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquiryConditions | Yield |
---|---|
With sodium hydroxide at 70℃; for 4h; Temperature; Large scale; | 97.57% |
Conditions | Yield |
---|---|
In water at 60℃; for 3h; | 94.4% |
Conditions | Yield |
---|---|
With lithium carbonate In ethanol at 20℃; for 6.5h; Heating; | 67% |
Conditions | Yield |
---|---|
In not given heated at 120°C for 2 h; recrystd. (C7H16); elem. anal.; hot-stage polarizing microscopy; DSC; |
rhodium (II) octanoate dimer
3-(piperidin-1-yl)-3-thioxopropanenitrile
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 24h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 24h; Inert atmosphere; | 100% |
rhodium (II) octanoate dimer
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 24h; Inert atmosphere; | 100% |
rhodium (II) octanoate dimer
3-(morpholin-4-yl)-3-thioxopropanenitrile
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 24h; Inert atmosphere; | 100% |
1-methyl-1H-pyrazole
rhodium (II) octanoate dimer
[Rh2(octanoato)4(1-methylpyrazole)]
Conditions | Yield |
---|---|
In chloroform (N2); a soln. of ligand added to Rh complex in CHCl3, stirred at room temp. for 1 h; evapd. (vac.); elem. anal.; | 99% |
1-methyl-1H-pyrazole
rhodium (II) octanoate dimer
[Rh2(octanoato)4(1-methylpyrazole)2]
Conditions | Yield |
---|---|
In chloroform (N2); a soln. of ligand added to Rh complex in CHCl3, stirred at room temp. for 1 h; evapd. (vac.); elem. anal.; | 99% |
rhodium (II) octanoate dimer
1-ferrocenyl-2-(4-pyridinyl)acetylene
Conditions | Yield |
---|---|
In dichloromethane all manipulations under oxygen- and water-free Ar atm.; soln. of Rh complex added to soln. of Fe complex, stirred at room temp. for 2 h; evapd. to dryness in vac., residue washed with n-hexane, recrystd. from Et2O, elem. anal.; | 86% |
rhodium (II) octanoate dimer
1,1’-di(4-(ethynyl)pyridine)ferrocene
Conditions | Yield |
---|---|
In dichloromethane all manipulations under oxygen- and water-free Ar atm.; Rh and Fe complexes dissolved in CH2Cl2, stirred at room temp. overnight; filtered, filtrate evapd. to dryness in vac., residue washed with Et2O, recrystd. by diffusion of Et2O into its CH2Cl2 soln., elem. anal.; | 86% |
rhodium (II) octanoate dimer
ferrocenyl-4-pyridine
Conditions | Yield |
---|---|
In dichloromethane all manipulations under oxygen- and water-free Ar atm.; Mo and Fe complexes dissolved in CH2Cl2, stirred at room temp. for 2 h; evapd. to dryness in vac., residue washed with n-hexane, recrystd. from CH2Cl2/n-hexane, elem. anal.; | 71% |
rhodium (II) octanoate dimer
[Fe(C5(C3H2N2CH3)5)(C5H4PO(t-C4H9)2)]*(chloroform)
Conditions | Yield |
---|---|
In acetonitrile (N2); Fe complex in MeCN added dropwise to a soln. of Rh complex, stirred at room temp. for 0.5 h; filtered, washed (MeCN, ether), dried in vac. at 60°C overnight; elem. anal.; | 64% |
rhodium (II) octanoate dimer
i-propyl nitrite
benzhydryl 6-aminopenicillanate
benzhydryl 6-oxopenicillanate
Conditions | Yield |
---|---|
With trifluoroacetic acid; methyloxirane In dichloromethane; ethyl acetate; benzene |
rhodium (II) octanoate dimer
Conditions | Yield |
---|---|
In ethyl acetate |
Conditions | Yield |
---|---|
In toluene byproducts: [(CH3)3CNH3][C7H15CO2], B2H6, H2; (N2); solutions of rhodium salt and tert-butylamine-borate in toluene were combinea at 25.0+-0.1°C, stirred for 2 h; concd., cold hexane was added, filtered, washed with hexane, dried in vac., elem. anal.; |
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