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16892-64-1

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16892-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16892-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,9 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16892-64:
(7*1)+(6*6)+(5*8)+(4*9)+(3*2)+(2*6)+(1*4)=141
141 % 10 = 1
So 16892-64-1 is a valid CAS Registry Number.
InChI:InChI=1/6CH3.3S.3Sn/h6*1H3;;;;;;/rC6H18S3Sn3/c1-10(2)7-11(3,4)9-12(5,6)8-10/h1-6H3

16892-64-1SDS

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 DIMETHYLTIN SULFIDE tech-95

1.2 Other means of identification

Product number -
Other names trimeric dimethyltin sulfide

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:16892-64-1 SDS

16892-64-1Related news

Interaction of DIMETHYLTIN SULFIDE (cas 16892-64-1) with 1,2-dibromoethane. Crystal structure of the dimethyltin dibromide /1,4-dithiane complex.08/02/2019

Reaction between trimeric dimethyltin sulfide and 1,2-dibromoethane of 140°C results in a complex of dimethyltin dibromide with 1,4-dithiane formulated as: Me2SnBr2 · SC2H4C2H4S · Me2SnBr2. X-ray analysis of the crystal structure of this complex has been performed.detailed

16892-64-1Relevant articles and documents

A New Route to Tris(dimethyltin sulphide) with Tetramethyltin as Co-product; the Wider Implications of This and Some Other Reactions leading to Tetramethyl-tin and -lead from Iodomethane

Craig, Peter J.,Rapsomanikis, Spyridon

, p. 114 (1982)

We describe a new light-promoted rearrangement of (Me3Sn)2S leading to cyclic (Me2SnS)3 and Me4Sn which has an important implication for the methylation of heavy metals in the environment and we also note some reactions of the natural product iodomethane leading to tetramethyl-tin and -lead.

Reaction of Trimeric Dimethyltin Sulfide with Sodium 4,N-Dichlorobenzenesulfamidate

Shcherbakov,Basova

, p. 1049 - 1053 (2007/10/03)

Reaction of the trimeric cyclic dimethyltin sulfide (Me2SnS)3 with sodium 4,N-dichlorobenzenesulfamidate (Khloramin-KhB) at a 1:2 molar ratio in anhydrous methanol first results in clevage of the six-membered ring with Khloramin-KhB and release of one of the three sulfur atoms in the form of S0 (oxidative degradation). The second stage involves oxidative imination of one of the two remaining sulfur atoms in the resulting acyclic compound with a second Khloramin-KhB molecule to give organotin sufimide, including a -Me2SnS(=NSO2C6H4Cl 4)SnMe2- functional fragment. Hydrolysis of this sulfimide gives 4-chlorobenzenesulfamide and the sulfite HO-Me2Sn-O-S(=O)-O-SnMe2-OH.

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