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2,3,4,4',5,6-HEXACHLOROBIPHENYL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41411-63-6

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41411-63-6 Usage

Uses

2,3,4,4'',5,6-Hexachlorobiphenyl is a polychlorinated biphenyl (PCB) congeners.

Check Digit Verification of cas no

The CAS Registry Mumber 41411-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,1 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41411-63:
(7*4)+(6*1)+(5*4)+(4*1)+(3*1)+(2*6)+(1*3)=76
76 % 10 = 6
So 41411-63-6 is a valid CAS Registry Number.

41411-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,4',5,6-Hexachlorobiphenyl

1.2 Other means of identification

Product number -
Other names 1,2,3,4,5-pentachloro-6-(4-chlorophenyl)benzene

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:41411-63-6 SDS

41411-63-6Downstream Products

41411-63-6Relevant academic research and scientific papers

Physical, spectral and chromatographic properties of all 209 individual PCB congeners

Bolgar,et al.

, p. 2687 - 2705 (2007/10/03)

Through the use of two capillary GC columns: 40% octadecyl/ 15% phenyl methyl siloxane and 50% phenyl methyl siloxane, it was possible to separate 201 PCB congeners with only four unresolved pairs. The data compiled in this study for all 209 congeners will aid in the identification of selected individual components of these environmental pollutants. The use of this data also presents the opportunity for the improved quantification of the commercial PCB formulations. -from Authors

Aryl(pentachlorophenyl)nickel(II) complexes. Lack of free rotation about tolyl-nickel bonds and lack of ortho effect in carbonylation

Wada, Masanori,Kusabe, Koji,Oguro, Keisuke

, p. 446 - 449 (2007/10/13)

A series of complexes of the type trans-R(C6Cl5)Ni(PPhMe2)2 (where R = aryl) was prepared. Their 1H NMR spectra indicate that both R = o-tolyl and m-tolyl groups are oriented perpendicularly to the nickel coordination plane. Reaction of carbon monoxide with these complexes gave, under mild conditions, R(C6Cl5)CO for R = aryl groups including o-tolyl but not for 2-furyl and its analogues. The o-tolyl complex was exceptionally stable toward thermal reductive elimination in tetrachloroethylene under air. Factors affecting the relative reactivities of these complexes are discussed, based mainly on the early explanation for the so-called ortho effect .

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