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Triphenylbismuth dibenzoate is a chemical compound with the formula (C6H5)3Bi(C7H5O2). It is a derivative of triphenylbismuth, where one of the phenyl groups is replaced by a dibenzoate ligand. triphenylbismuth dibenzoate is characterized by its stability and is often used in organic synthesis as a bismuth source. It is also known for its potential applications in materials science, particularly in the development of new catalysts and as a precursor for the synthesis of other organobismuth compounds. The compound's structure provides insight into the coordination chemistry of bismuth, which is of interest in the field of inorganic chemistry.

57997-58-7

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57997-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57997-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,9 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57997-58:
(7*5)+(6*7)+(5*9)+(4*9)+(3*7)+(2*5)+(1*8)=197
197 % 10 = 7
So 57997-58-7 is a valid CAS Registry Number.

57997-58-7Relevant academic research and scientific papers

Thermodynamic Properties of Triphenylbismuth Dibenzoate Ph3Bi(OC(O)Ph)2 and Triphenylantimony Dibenzoate Ph3Sb(OC(O)Ph)2

Gushchin, A. V.,Lyakaev, D. V.,Markin, A. V.,Sharutin, V. V.,Sharutina, O. K.,Smirnova, N. N.

, p. 2207 - 2213 (2021/11/11)

Abstract: The temperature dependence of the heat capacity of triphenylbismuth dibenzoate Ph3Bi(OC(O)Ph)2 is measured for the first time in the range of Т = (6 and 480) K using precision adiabatic vacuum and differential scanning calo

Study of homo- and cross-coupling competition in the reaction of triarylbismuth(V) dicarboxylates with methyl acrylate in the presence of a palladium catalyst

Moiseev, Dmitry V.,Malysheva, Yulia B.,Shavyrin, Andrey S.,Kurskii, Yury A.,Gushchin, Aleksey V.

, p. 3652 - 3663 (2007/10/03)

Triarylbismuth(V) derivatives Ar3Bi(O2CR)2 (Ar = Ph, m-Tol, p-Tol; R = H, Me, Et, n-Bu, t-Bu, n-C5H 11, CF3, CH2Cl, CCl3, Ph) were prepared in good to excellent yields by reaction of Ar3Bi with equimolar amounts of t-BuOOH in the presence of an acid. These compounds were tested in the C-arylation reaction of methyl acrylate, as a model substrate, in the presence of palladium catalyst (4 mol%). It was found that triphenylbismuth dicarboxylates are very active phenylating agents under mild conditions (20 °C). The effect of the carboxylic group, the effect of the nature of the palladium catalyst and the effect of oxygen on the reactivity of the organobismuth compounds and on the selectivity of the C-arylation reaction were studied. Methyl cinnamate, the C-phenylation product, and biphenyl, the homo-coupling by-product, were obtained in all cases. Triphenylbismuth divalerate Ph3Bi(O2CBu)2 is the most reactive compound among the triphenylbismuth dicarboxylates studied.

Reaction of pentaphenylantimony with triphenylbismuth diacylates

Sharutin,Sharutina,Egorova,Senchurin,Ivashchik,Bel'skii

, p. 873 - 875 (2007/10/03)

Reactions of pentaphenylantimony with triphenylbismuth diacylates yield the corresponding tetraphenylantimony acylates. Triphenylbismuth bis(trichloroacetate) was prepared by oxidation of triphenylbismuth with hydrogen peroxide in the presence of trichloroacetic acid. The structure of triphenylbismuth dibenzoate was determined by single crystal X-ray diffraction. The coordination polyhedron of the central atom is intermediate between trigonal bipyramid and pentagonal bipyramid; the benzoate groups occupy the equatorial position.

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