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4,5-DIIODO-PHTHALIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82679-28-5

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82679-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82679-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,7 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82679-28:
(7*8)+(6*2)+(5*6)+(4*7)+(3*9)+(2*2)+(1*8)=165
165 % 10 = 5
So 82679-28-5 is a valid CAS Registry Number.

82679-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-diiodophthalic acid

1.2 Other means of identification

Product number -
Other names 4,5-Dijod-phthalsaeure

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:82679-28-5 SDS

82679-28-5Relevant academic research and scientific papers

Facile Synthesis, Triplet-State Properties, and Electrochemistry of Hexaiodo-Subphthalocyanine

Ob?oza, Magdalena,?apok, ?ukasz,Solarski, J?drzej,P?dziński, Tomasz,Nowakowska, Maria

, p. 17080 - 17090 (2018/11/01)

In view of the ever-growing demand for efficient triplet photosensitizers and photoactive components of various optoelectronic devices, we herein report the synthesis and properties of hexaiodo-subphthalocyanines (I6SubPcs). The improved five-s

Control of the molecular packing of chloroboron(III) and fluoroboron(III) subnaphthalocyanines by designing peripheral substituents

Takagi, Akuto,Mizutani, Tadashi

, p. 54235 - 54245 (2017/12/05)

Chloroboron(iii) and fluoroboron(iii) hexa(1-alkynyl)- and hexa(2-arylethynyl)subnaphthalocyanines with a large dipole moment were prepared by Sonogashira coupling of hexaiodosubnaphthalocyanines with substituted acetylenes. Introduction of butyl or longe

Synthesis and optoelectronic properties of hexachloro- and hexaiodosubnaphthalocyanines as organic electronic materials

Yamamoto, Koji,Takagi, Akuto,Hada, Miyako,Taniwaki, Ryosuke,Mizutani, Tadashi,Kimura, Yoshifumi,Takao, Yuko,Moriwaki, Kazuyuki,Matsumoto, Fukashi,Ito, Takatoshi,Iwai, Toshiyuki,Hida, Koichi,Mizuno, Takumi,Ohno, Toshinobu

, p. 4918 - 4924 (2016/07/18)

Chloroboron(III) hexachloro- and hexaiodosubnaphthalocyanines were prepared, and their solubility, electronic absorption spectroscopy, fluorescence emission spectroscopy and HOMO/LUMO energy levels were evaluated. These subnaphthalocyanines showed lower H

Synthesis of hexadehydrotribenzo[a,e,i][12]annulenes by acetylene insertion into an open-chain precursor

Dudic, Miroslav,Cisarova, Ivana,Michl, Josef

experimental part, p. 68 - 74 (2012/03/10)

A simple synthesis of a hexadehydrotribenzo[a,e,i][12]annulene by insertion of acetylene into an open-chain diiodo precursor under Sonogashira coupling conditions has been developed and used to prepare a rigid three-armed star connector for testing as a b

Spectroscopic properties of macrocyclic oligo(phenyldiacetylenes)-II. Synthesis and theoretical study of diacetylenic dehydrobenzoannulene derivatives with weak electron-donor and -acceptor groups

Zimmermann, Boris,Baranovi?, Goran,?tefani?, Zoran,Ro?man, Marko

, p. 115 - 124 (2007/10/03)

Diacetylenic dehydrobenzo[12]annulene and dehydrobenzo[18]annulene derivatives with electron-donor and -acceptor groups were synthesized (including push-pull Eglinton-Galbraith dimer derivative 1c) via an oxidative coupling reaction, and spectroscopically

Design, synthesis, and properties of new derivatives of pentacene

Jiang, Jinyue,Kaafarani, Bilal R.,Neckers, Douglas C.

, p. 2155 - 2158 (2007/10/03)

Stable, soluble ethynylated derivatives of pentacene (9a-c) were synthesized, and the ethynyl moieties on the terminal rings were used to tune the electronic properties of these compounds. Their oxidation potentials are higher and their reduction potentia

Vibrational spectra of halophthalonitriles

Halls, Mathew D.,Aroca, Ricardo,Terekhov, Dmitri S.,D'Ascanio, Anna,Leznoff, Clifford C.

, p. 305 - 317 (2007/10/03)

The fundamental vibrational modes of a series of six halophthalonitriles have been studied using Raman and infrared spectroscopy. The vibrational assignment of experimental wave numbers obtained from solid samples was aided using quantum chemical computations. Semi-empirical methods and the local SVWN functional were used to obtain vibrational wave numbers and atomic displacement representations of the fundamental molecular vibrations. The study of a series of molecules with similar structure permits the identification of characteristic wave numbers and the effect of the halosubstitution in the molecular structure.

Synthesis of 2,3,9,10,16,17,23,24-octaalkynylphthalocyanines and the effects of concentration and temperature on their 1H NMR spectra

Terekhov, Dmitri S.,Nolan, Kieran J. M.,McArthur, Colin R.,Leznoff, Clifford C.

, p. 3034 - 3040 (2007/10/03)

The syntheses of 3,4- and 4,5-diiodophthalonitriles are described. Coupling of the latter compound with Pd(PPh3)2Cl2 and 1-octyne, 1-heptyne, 1-hexyne, 1-pentyne, and 3,3-dimethyl-1-butyne gave a series of 4,5-dialkynylphthalonitriles. Hydrogenation of 4,5-bis(1-pentynyl)phthalonitrile and 4,5-bis(3,3-dimethyl-1-butynyl)phthalonitrile gave 4,5-dipentylphthalonitrile and 4,5-bis(3,3-dimethylbutyl)phthalonitriles. Condensation of the dialkynylphthalonitriles with lithium 1-pentoxide in 1-pentanol gave 2,3,9,10,16,17,23,24-octaalkynylphthalocyanines, while intervention of the intermediate dilithium phthalocyanines with zinc acetate gave the related zinc(II) phthalocyanines. 1H NMR spectroscopy of these octaalkynylphthalocyanines exhibited large chemical shifts (1-2 ppm) of the internal and aromatic protons at concentrations ranging from 10-2 to 10-5 M and at temperatures from 27 to 147°C. The effects of aggregation phenomena are discussed. The importance of reporting concentration and temperature values for NMR spectra of phthalocyanines is stressed.

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