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tetraphenylstibonium acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75136-99-1

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75136-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75136-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,3 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75136-99:
(7*7)+(6*5)+(5*1)+(4*3)+(3*6)+(2*9)+(1*9)=141
141 % 10 = 1
So 75136-99-1 is a valid CAS Registry Number.

75136-99-1SDS

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 tetraphenylantimony benzoate

1.2 Other means of identification

Product number -
Other names -

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:75136-99-1 SDS

75136-99-1Relevant academic research and scientific papers

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.

Synthesis and thermal decomposition of derivatives of acyloxytetraphenylantimony

Sharutina,Sharutin,Senchurin,Fukin,Zakharov,Yanovsky,Struchkov

, p. 186 - 190 (2007/10/03)

Acyloxy derivatives of tetraphenylantimony of the general formula Ph4SbOC(O)R (R = Alk or Ar) have been synthesized by the reaction of pentaphenylantimony with carboxylic acids. Thermolysis of the compounds obtained affords phenyl carboxylates and triphenylstibine in quantitative yields. One of these compounds (R = CH=CHPh) has been studied by X-ray structural analysis. In this compound, the Sb atom has a trigonal-bipyramidal coordination. The Sb-O(Ph)eq distances are in the range 2.103(4)-2.140(5) A; the Sb-C(Ph)ax bond length is 2.167(5) A. The fragment of the residue of cinnamic acid has a delocalized double bond in the carboxylate group.

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