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

4342-36-3

4342-36-3 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

4342-36-3 Usage

Uses

Agricultural chemical.

Hazard

A poison by ingestion.

Safety Profile

Poison by ingestion andintravenous routes. Moderately toxic by subcutaneousroute. When heated todecomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 4342-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4342-36:
(6*4)+(5*3)+(4*4)+(3*2)+(2*3)+(1*6)=73
73 % 10 = 3
So 4342-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6O2.3C4H9.Sn/c8-7(9)6-4-2-1-3-5-6;3*1-3-4-2;/h1-5H,(H,8,9);3*1,3-4H2,2H3;/q;;;;+1/p-1/rC12H27Sn.C7H6O2/c1-4-7-10-13(11-8-5-2)12-9-6-3;8-7(9)6-4-2-1-3-5-6/h4-12H2,1-3H3;1-5H,(H,8,9)/q+1;/p-1

4342-36-3SDS

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 tributylstannyl benzoate

1.2 Other means of identification

Product number -
Other names Caswell No. 867AA

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:4342-36-3 SDS

4342-36-3Relevant academic research and scientific papers

N-Heterocyclic carbene catalyzed oxidative stannylation of aldehydes: A facile entry to organotin(IV) carboxylates

Reddi, Rambabu N.,Malekar, Pushpa V.,Sudalai, Arumugam

, p. 2679 - 2681 (2013/06/05)

A simple protocol is described for the oxidative transformation of aldehydes to the corresponding organotin(IV) carboxylates in high yields (up to 90%) that utilizes atmospheric O2 as the sole oxidant, N-heterocyclic carbene as catalyst (at 10 mol %), and tributyl tin chloride as stannylating agent. The uniqueness of the reaction lies in the direct conversion of aldehydes to the corresponding organotin(IV) carboxylates via stannylation of carboxylic acids, generated from the reaction of a Breslow intermediate with O2.

Synthesis, characterization and in vitro antitumour activity of triphenyl- and tri-n-butyltin benzoates, phenylacetates and cinnamates

Willem, Rudolph,Bouhdid, Abdeslam,Mahieu, Bernard,Ghys, Laurent,Biesemans, Monique,Tiekink, Edward R.T.,De Vos, Dick,Gielen, Marcel

, p. 151 - 158 (2007/10/03)

Spectroscopic, structural and antitumour properties of triphenyltin and tri-n-butyltin benzoates, phenylacetates and cinnamates are compared with those of their corresponding pentafluorophenyl analogues.

Triorganotin(IV) Benzoates and Aminobenzoates

Sandhu, G. K.,Verma, S. P.,Moore, L. S.,Parish, R. V.

, p. 15 - 26 (2007/10/02)

Complexes of the general formula R3SnX, where X is the anion of benzoic acid, o-, m-, p-amino- or N-phenyl-o-amino-benzoic acid, have been prepared and characterised.A combination of molecular weight, infrared, 1H NMR and 119Sn Moessbauer measurements show that, the amino-nitrogen atoms are not coordinated to tin.When R= phenyl or cyclohexyl, the compounds are monomeric and four-coordinate, and when R is alkyl (Me, n-Pr, n-Bu) they are monomeric and five-coordinate, with a bidentate carboxylate in the equatorial position of a trigonal bipyramidal structure.

FREE RADICAL CHAIN REACTION OF ALLYLIC TIN COMPOUNDS WITH ORGANIC HALIDES INVOLVING SH prime PROCESS.

Migita,Nagai,Kosugi

, p. 2480 - 2484 (2007/10/02)

Negatively substituted halomethanes were allylated easily by allyltin compounds via radical chain reaction involving S//H prime process. Aryl, aralkyl, and alkyl halides underwent similar chain reactions only when the tin compound was charged in excessive amounts.