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Stannane, dibutylbis[(4-chlorobenzoyl)oxy]-, also known as dibutyltin bis(4-chlorobenzoate), is an organotin compound with the chemical formula C22H34Cl2O4Sn. It is a colorless to pale yellow liquid with a molecular weight of 565.04 g/mol. Stannane, dibutylbis[(4-chlorobenzoyl)oxy]- is primarily used as a catalyst in the production of polyurethane foams and as a stabilizer in various polymers. It is also employed in the synthesis of other organotin compounds. Due to its potential environmental and health risks, its use is regulated in some regions.

7580-79-2

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7580-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7580-79-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,8 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7580-79:
(6*7)+(5*5)+(4*8)+(3*0)+(2*7)+(1*9)=122
122 % 10 = 2
So 7580-79-2 is a valid CAS Registry Number.

7580-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [dibutyl-(4-chlorobenzoyl)oxystannyl] 4-chlorobenzoate

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

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More Details:7580-79-2 SDS

7580-79-2Downstream Products

7580-79-2Relevant academic research and scientific papers

A novel synthetic method of 2,4-disubstituted oxazoles using carboxylic acid-derived Bu2Sn[OC(O)R]2

Yoneyama, Hiroki,Oka, Naoki,Usami, Yoshihide,Harusawa, Shinya

supporting information, (2020/05/21)

A novel synthetic method for the preparation of 2,4-disubstituted oxazoles was developed, entailing the reaction of dibutyltin diacylates Bu2Sn[OC(O)R]2 with 1-substituted acetylenes and TMSN3 to afford a range of 2,4-disu

The synthesis, characterization and comparative anticorrosion study of some organotin(IV) 4-chlorobenzoates

Kurniasih, Hastin,Nurissalam, Muhamad,Iswantoro, Bambang,Afriyani, Hapin,Qudus, Hardoko Insan,Hadi, Sutopo

, p. 2377 - 2383 (2016/02/27)

The synthesis of 3 compounds of a series of dibutyl(IV) di-4-chlorobenzoate, diphenyl(IV) di-4-chlorobenzoate and triphenyltin(IV) 4-chlorobenzoate have successfully been performed by reacting the dibutyltin(IV) dichloride, diphenyltin(IV) dichloride and triphenyltin(IV) chloride respectively via the dibutyltin(IV) oxide, diphenyltin(IV) dihydroxide and triphenyltin(IV) hydroxide with 4-chlorobenzoic acid. All compounds synthesized were well characterized by 1H and 13C NMR, IR and UV-Vis spectroscopies as well as based on the microanalytical data. The anticorrosion activity of these compounds were tested on Hot Roller Plate (HRP) mild steel in DMSO-HCl solution using potentiodynamic method. The results revealed that the triphenyltin(IV) 4-chlorobenzoate clearly showed the strongest inhibitor activity compared to the other derivatives, while diphenyltin(IV) compounds were better than that of dibutyltin(IV) analogous. The results reported here indicated that the optimal activity were depended on the ligand attached to the metal centre and might also be related to the number of carbon atoms present in the organotin(IV) used.

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