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TRIPHENYLANTIMONY(V) DIBENZOATE 97 is a chemical compound belonging to the antimony family, featuring triphenylantimony and dibenzoate groups. It is recognized for its effectiveness as a catalyst in organic reactions, particularly in esterification and transesterification processes, due to its ability to promote bond formation between molecules. TRIPHENYLANTIMONY(V) DIBENZOATE 97 is a valuable and versatile tool in organic synthesis, known for delivering high yields and selectivity in a range of reactions. However, it is crucial to handle TRIPHENYLANTIMONY(V) DIBENZOATE 97 with caution due to its potential toxicity and harmful effects if ingested or inhaled.

57997-56-5

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57997-56-5 Usage

Uses

Used in Organic Synthesis Industry:
TRIPHENYLANTIMONY(V) DIBENZOATE 97 is used as a catalyst for facilitating esterification and transesterification processes in organic synthesis. It is chosen for its ability to enhance the formation of bonds between molecules, leading to high yields and selectivity in various chemical reactions.
Used in Catalyst Applications:
In the field of catalysis, TRIPHENYLANTIMONY(V) DIBENZOATE 97 serves as an effective agent in promoting chemical reactions, making it a preferred choice for researchers and chemists working on improving reaction efficiency and product quality. Its versatility in catalytic processes underscores its importance in advancing organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 57997-56-5 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 57997-56:
(7*5)+(6*7)+(5*9)+(4*9)+(3*7)+(2*5)+(1*6)=195
195 % 10 = 5
So 57997-56-5 is a valid CAS Registry Number.

57997-56-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [benzoyloxy(triphenyl)-λ<sup>5</sup>-stibanyl] benzoate

1.2 Other means of identification

Product number -
Other names triphenylantimony bisbenzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57997-56-5 SDS

57997-56-5Relevant academic research and scientific papers

Thermochemical Properties of Triphenylantimony Dibenzoate Ph3Sb(OC(O)Ph)2

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

, p. 1776 - 1779 (2020)

Abstract: The energy of combustion of crystalline triphenylantimony dibenzoate is measured using an isoperibolic combustion calorimeter with a static bomb at T = 298.15 K. The experimental data show that the standard enthalpy of combustion of this substance in the crystalline state is calculated for T = 298.15 K. Standard functions ?fH° and ?fG° of the formation of the compound in the crystalline state are calculated for T = 298.15 K.

Thermodynamic properties of triphenylantimony dibenzoate

Markin,Smirnova,Lyakaev,Klimova,Sharutin,Sharutina

, p. 1913 - 1920 (2016)

The temperature dependence of the heat capacity of triphenylantimony dibenzoate Ph3Sb(OC(O)Ph)2 is studied in the range of 6–480 K by means of precision adiabatic vacuum calorimetry and differential scanning calorimetry. The melting of the compound is observed in this temperature range, and its standard thermodynamic characteristics are identified and analyzed. Ph3Sb(OC(O)Ph)2 is obtained in a metastable amorphous state in a calorimeter. The standard thermodynamic functions of Ph3Sb(OC(O)Ph)2 in the crystalline and liquid states are calculated from the obtained experimental data: Cp °(T), H°(T)–H°(0), S°(T), and G°(T)–H°(0) for the region from T → 0 to 480 K. The standard entropy of formation of the compound in the crystalline state at T = 298.15 K is determined. Multifractal processing of the low-temperature (T a planar chain topology.

Synthesis and Structure of Triarylantimony Bis(arenesulfonates)

Sharutin,Sharutina,Platonova,Pakusina,Panova,Fukin,Zakharov

, p. 354 - 357 (2007/10/03)

Triarylantimony bis(arenesulfonates) were prepared by reaction of triarylantimonies with hydrogen peroxide in the presence of arenesulfonic acids. The steric structure of the products was assessed. Triarylantimony bis(arenesulfonates) were reacted with so

Pd-catalyzed C-arylation of unsaturated compounds with pentavalent triarylantimony dicarboxylates

Moiseev, Dmitry V.,Gushchin, Aleksey V.,Shavirin, Andrey S.,Kursky, Yury A.,Dodonov, Viktor A.

, p. 176 - 184 (2007/10/03)

Triarylantimony (V) derivatives Ar3SbX2 (X = Hal or acyloxy) were prepared by reaction of Ar3Sb with equimolar amounts of a peroxide ROOH (R = t-Bu, H) in the presence of an acid or an anhydride in good to excellent yields. Ar3Sb(O2CR)2 are mild and efficient C-arylation reagents of unsaturated compounds (methyl acrylate, styrene, 2-phenylpropene and acrylonitrile) under palladium catalysis at 50 °C, with PdCl2 being the most effective catalyst. Ar3SbHal2 do not react under these conditions.

Electrochemistry of hypervalent compounds - V. Anodic oxidation of trivalent organoantimony and organobismuth compounds

Fuchigami, Toshio,Miyazaki, Motoko

, p. 1979 - 1984 (2008/10/08)

Anodic oxidation of triphenylantimony in the presence of various oxygen nucleophiles or halide ions provided the corresponding hypervalent compounds having Sb - Y bonds (Y = RCOO, F, Cl, Br) in good yields. On the contrary, anodic oxidation of triphenylbi

Synthesis of triphenylantimony (hydroxo)diketonates by oxidative methods

Gushchin, A. V.,Dodonov, V. A.,Usyatinsky, R. I.,Koreshkova, E. R.,Tipanov, B. B.

, p. 1239 - 1241 (2007/10/02)

Triphenylantimony (hydroxo)acetylacetonate, (hydroxo)trifluoroacetylacetonato, and (hydroxo)pivaloyltrifluoroacetonato were prepared in 85-98percent yields by oxidation of triphenylantimony with hydrogen peroxide or tert-butyl hydroperoxide in the presenc

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