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μ-oxo-bis[tris(cyclohexyl)chloroantimony(V)] is a complex organoantimony compound characterized by its unique structure and properties. This chemical features a central μ-oxo bridge connecting two antimony atoms, each of which is bonded to three cyclohexyl groups and a chlorine atom, resulting in the formula [Sb(C6H11)3Cl]2O. It is a yellow crystalline solid with potential applications in various chemical reactions and as a precursor for the synthesis of other antimony-containing compounds. Due to its stability and reactivity, it is of interest to researchers in the field of organometallic chemistry and materials science.

85372-04-9

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85372-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85372-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85372-04:
(7*8)+(6*5)+(5*3)+(4*7)+(3*2)+(2*0)+(1*4)=139
139 % 10 = 9
So 85372-04-9 is a valid CAS Registry Number.

85372-04-9Relevant academic research and scientific papers

The Preparation of (C6H11)3Sb(OH)Y and Their Infrared Spectra

Kawasaki, Yoshikane,Yamamoto, Yasushi,Wada, Masanori

, p. 145 - 148 (1983)

Tris(cyclohexyl)hydroxoantimony(V) compounds, (C6H11)3Sb(OH)Y, Y=Cl, Br, CH3COO, and NO3, were prepared by the hydrolysis of μ-oxo-bis, 2O, in a mixed solvent of acetone and water(7:3) or by a reaction of silver salts with 2O in the same solvent.When Y=Cl and Br, the dehydration of the hydroxo compounds, giving the μ-oxo compounds, 2O, occurred readily.However, when Y=CH3COO and NO3, the hydroxo form is stable.In the IR spectra of these hydroxo compounds in dichloromethane solution, the ν(O-H) band was observed at ca. 3630 cm-1 and the ν(SbO) band, at 565-513 cm-1.The hydrolysis of several μ-oxo compounds, 2O, R=CH3, C2H5, i-C3H7, C6H5, and p-CH3C6H4, Y=Cl, Br, CH3COO, and NO3, in a water-saturated dichloromethane solution was studied by using the IR spectra.All the compounds were hydolyzed in this solvent, but only the starting μ-oxo compounds were recovered from this solution.

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