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5,6,12,13-tetrachloroanthra(2,1,9-def:6,5,10-d'e'f')diisoquinoline-1,3,8,10(2H,9H)-tetrone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115662-06-1

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115662-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115662-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,6 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115662-06:
(8*1)+(7*1)+(6*5)+(5*6)+(4*6)+(3*2)+(2*0)+(1*6)=111
111 % 10 = 1
So 115662-06-1 is a valid CAS Registry Number.

115662-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6,7,12-tetrachloroperylen-3,4:9,10-tetracarboxylic acid diimide

1.2 Other means of identification

Product number -
Other names 1,6,7,12-Tetrachloro-3,4,9,10-tetracarboxylicacid diimide

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:115662-06-1 SDS

115662-06-1Downstream Products

115662-06-1Relevant academic research and scientific papers

Self-assembly of twisted tetrachloroperylenediimide chromophores into two dimensional brick-stone aggregates: Exciton dynamics and photoconductivity

Cao, Xinqiang,Bai, Shuming,Wu, Yishi,Liao, Qing,Shi, Qiang,Fu, Hongbing,Yao, Jiannian

, p. 6402 - 6404 (2012)

2D self-assembly has been demonstrated in perylenediimides with twisted chromophores, in which the π-π stacked units are interconnected via hydrogen bonding interactions. Spectroscopic measurements and theoretical calculations suggest a weak J-type exciton coupling in the assembly. High photoconductivity of the 2D crystal makes it a promising candidate for further opto-electronic applications.

Method for producing organic field-effect transistors

-

Page/Page column 38-39, (2011/04/18)

A method for producing an organic field-effect transistor, comprising the steps of: a) providing a substrate comprising a gate structure, a source electrode and a drain electrode located on the substrate, andb) applying an n-type organic semiconducting compound to the area of the substrate where the gate structure, the source electrode and the drain electrode are located, wherein the n-type organic semiconducting compound is selected from the group consisting of compounds of the formula I wherein R1, R2, R3and R4are independently hydrogen, chlorine or bromine, with the proviso that at least one of these radicals is not hydrogen,Y1 is O or NRa, wherein Ra is hydrogen or an organyl residue,Y2 is O or NRb, wherein Rb is hydrogen or an organyl residue,Z1, Z2, Z3 and Z4 are O, where, in the case that Y1 is NRa, one of the residues Z1 and Z2 may be a NRc group, where Ra and Rc together are a bridging group having 2 to 5 atoms between the terminal bonds, where, in the case that Y2 is NRb, one of the residues Z3 and Z4 may be a NRd group, where Rb and Rd together are a bridging group having 2 to 5 atoms between the terminal bonds.

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