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2767-47-7

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2767-47-7 Usage

Chemical Properties

White crystalline powder

Safety Profile

Poison by intravenous route. When heated to decomposition it emits toxic fumes of Br-. See also TIN COMPOUNDS and BROMIDES.

Check Digit Verification of cas no

The CAS Registry Mumber 2767-47-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2767-47:
(6*2)+(5*7)+(4*6)+(3*7)+(2*4)+(1*7)=107
107 % 10 = 7
So 2767-47-7 is a valid CAS Registry Number.
InChI:InChI=1/2CH3.2BrH.Sn/h2*1H3;2*1H;/q;;;;+2/p-2/rC2H6Sn.2BrH/c1-3-2;;/h1-2H3;2*1H/q+2;;/p-2

2767-47-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A18060)  Dimethyltin dibromide, 98%   

  • 2767-47-7

  • 5g

  • 1216.0CNY

  • Detail
  • Alfa Aesar

  • (A18060)  Dimethyltin dibromide, 98%   

  • 2767-47-7

  • 25g

  • 4887.0CNY

  • Detail

2767-47-7SDS

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 dibromo(dimethyl)stannane

1.2 Other means of identification

Product number -
Other names dibromodimethylstannane

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:2767-47-7 SDS

2767-47-7Relevant articles and documents

INTERACTION OF DIMETHYLTIN SULFIDE WITH 1,2-DIBROMOETHANE. CRYSTAL STRUCTURE OF THE DIMETHYLTIN DIBROMIDE/1,4-DITHIANE COMPLEX

Shcherbakov, V. I.,Grigor'eva, I. K.,Razuvaev, G. A.,Zakharov, L. N.,Bochkova, R. I.,Struchkov, Yu. T.

, p. 41 - 48 (1987)

Reaction between trimeric dimethyltin sulfide and 1,2-dibromoethane at 140 degC 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.

Selective and sequential reduction of polyhalosilanes with alkyltin hydrides

D'Errico, John J.,Sharp, Kenneth G.

, p. 2177 - 2180 (2008/10/08)

The reactions between alkyltin hydrides and a variety of polyhalo- and mixed halosilanes have been investigated. For SiCl4 and SiCl3H, the reductions proceed in a stepwise manner to yield the monoreduced species as the major products. The reduction of SiBr4 occurs much faster to yield a mixture of SiBr3H and SiH4, or, in the vapor phase, SiBr3H as the sole product. SiF3X (X = Br, Cl) is converted into SiF3H, with no further reduction of SiF3H observed upon addition of a second equivalent of alkyltin hydride. SiF2HX compounds (X = Br, Cl) are obtained from SiF2X2 and are converted into SiF2H2 with excess Me3SnH. Redistribution becomes competitive with reduction in reactions between Me3SnH and SiFBr3, leading to mixtures of SiH4, SiF2H2, and SiF3H. The major products in the reaction between SiCl2Br2 and Me3SnH are SiCl3H and SiH4 (no SiCl2H2 was observed). Several probable intermediates were independently synthesized and allowed to react with Me3SnH. Together with deuterium labeling experiments, these reactions shed light on the mechanisms involved in these systems. In particular, the reactions appear not to proceed via free radicals.

Electrophilic cleavages in (CH3)3SnCH2M(CH3)3 (M = Sn, Ge, Si, C). 1. Product distribution

Hawker, Darryl W.,Wells, Peter R.

, p. 821 - 825 (2008/10/08)

The extent to which Sn-CH2 and/or Sn-CH3 cleavage occurs in (CH3)3SnCH2M(CH3)3 (M = Sn, Ge, Si) in reactions with several electrophiles has been determined. With iodine and with

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