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103426-96-6

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103426-96-6 Usage

Uses

1,2,3,4,6,7-Hexachloronaphthalene is a persistent organohalogenated pollutant found in the air and wastewater.

Check Digit Verification of cas no

The CAS Registry Mumber 103426-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,2 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103426-96:
(8*1)+(7*0)+(6*3)+(5*4)+(4*2)+(3*6)+(2*9)+(1*6)=96
96 % 10 = 6
So 103426-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H2Cl6/c11-5-1-3-4(2-6(5)12)8(14)10(16)9(15)7(3)13/h1-2H

103426-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,6,7-Hexachloronaphthalene

1.2 Other means of identification

Product number -
Other names LS-2269

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:103426-96-6 SDS

103426-96-6Downstream Products

103426-96-6Relevant articles and documents

Synthesis and Crystallography of 1,2,3,4,6,7-Hexachloronaphthalene and 1,2,3,5,6,7-Hexachloronaphthalene

Jakobsson, Eva,Eriksson, Lars,Bergman, Ake

, p. 527 - 532 (2007/10/02)

1,2,3,4,6,7-Hexachloronaphthalene (5) and 1,2,3,5,6,7-hexachloronaphthalene (6) have been synthesized via reductive dehalogenation of octachloronaphthalene by lithium aluminium hydride.The reduction proceeds via the substitution of one of the chlorine atoms in an α-position and the formation of 1,2,3,4,5,6,7-heptachloronaphthalene (4).The two sterically more crowded α-positions (positions four and five) in the heptachloronaphthalene were found to be preferentially reduced as the reduction proceeds.Only trace amounts of other isomers were formed.Crystal and molecular structure of the two title isomers were determined by single crystal X-ray diffraction methods.The compounds crystallize in the space group P21/c with the following cell dimensions: 5, a = 14.71(2) Angstroem, b = 3.828(4) Angstroem, c = 20.45(3) Angstroem, and β = 87.8(1) deg; 6, a = 9.381(4) Angstroem, b = 3.807(2) Angstroem, c = 16.168(8) Angstroem and β = 102.40(4) deg.The structures were determined by direct methods and the obtained models containing total of 95 parameters for 5 and 48 parameters for 6 were refined by full-matrix least-squares calculations that gave a final R value of: 5, 0.0619 for 486 unique reflections with I/?(I) 3 and 6, 0.0592 for 382 unique reflections with I/?(I) 3.

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