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Tris(cyclohexyl)acetatohydroxoantimony(V) is a complex organoantimony compound with the chemical formula [Sb(OC6H11)3(OH)(O2CCH3)]n. It consists of antimony (Sb) in the +5 oxidation state, three cyclohexyl groups (C6H11), one hydroxyl group (OH), and one acetate group (O2CCH3). tris(cyclohexyl)acetatohydroxoantimony(V) is characterized by its unique structure, where the antimony atom is coordinated to three cyclohexyl groups, one hydroxyl group, and one acetate group, forming a pentacoordinate geometry. Tris(cyclohexyl)acetatohydroxoantimony(V) is of interest in organometallic chemistry and has potential applications in various fields, such as catalysis and material science.

85362-34-1

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85362-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85362-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,6 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85362-34:
(7*8)+(6*5)+(5*3)+(4*6)+(3*2)+(2*3)+(1*4)=141
141 % 10 = 1
So 85362-34-1 is a valid CAS Registry Number.

85362-34-1Relevant 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 (2007/10/02)

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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