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Benzene, 1,1'-[(1E)-1,2-dichloro-1,2-ethenediyl]bis[2,3,4,5,6-pentachloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52789-10-3

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52789-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52789-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52789-10:
(7*5)+(6*2)+(5*7)+(4*8)+(3*9)+(2*1)+(1*0)=143
143 % 10 = 3
So 52789-10-3 is a valid CAS Registry Number.

52789-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-perchlorostilbene

1.2 Other means of identification

Product number -
Other names Perchlor-trans-stilben

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:52789-10-3 SDS

52789-10-3Downstream Products

52789-10-3Relevant academic research and scientific papers

Influence of elemental sulfur on the de-novo-synthesis of organochlorine compounds from residual carbon on fly ash

Bechtler,Stieglitz,Zwick,Will,Roth,Hedwig

, p. 2261 - 2278 (2007/10/03)

Thermal experiments between 300°C and 500°C were performed with fly ash of a municipal waste incineration plant which had been spiked with elemental sulfur. The influence of elemental sulfur on the heterogeneous carbon-decomposition and the de-novo-synthesis of polychlorinated compounds was investigated. Compounds such as polychlorinated dibenzodioxins, dibenzofurans, benzenes, benzoand dibenzothiophenes, Cl4-thiophene, Cl4- thienothiophene, Cl7- and Cl8-phenylthiophene were quantified. Apart from those, other intermediate structures were determined. These compounds are mainly aromatics with a vinyl- or butadienyl-group, stabilized by perchlorination. In detail, the compounds are Cl7- and Cl8-styrene, Cl10-vinylnaphthalenes, Cl10-phenylbutadiene, Cl10-octatetraene, Cl10-bis-butadienylsulfides and Cl12-stilbenes.

A New Synthesis, Chemical Behavior, and Spectra of Perchlorodiphenylacetylene

Ballester, M.,Castaner, J.,Riera, J.,Armet, O.

, p. 1100 - 1105 (2007/10/02)

A new, high-yield synthesis of perchlorodiphenylacetylene (2) by dechlorination of cis-perchlorostilbene (1a) with Cu at 310 deg C is described.The photochemical reaction of tolane 2 with Cl2 or tetrachloroethylene affords trans-perchlorostilbene (1b) or

PERCHLOROTOLANE. A NEW SYNTHESIS AND ITS THERMAL DIMERIZATION

Ballester, M.,Castaner, J.,Riera, J.,Armet, O.

, p. 2845 - 2848 (2007/10/02)

A new synthesis of perchlorotolane (perchlorodiphenylacetylene; I) is described.It dimerizes at high temperature to give perchloro-1,2,3-triphenyl-naphthalene (III) and perchloro-2,3,8-triphenylbenzofulvene (IV).Under the same conditions the latter yields

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