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1,2-Benzenedicarbonitrile, 4,5-dibromo-3,6-dihydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4593-01-5

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4593-01-5 Usage

Physical state

Yellow crystalline solid

Uses

a. Manufacture of pigments
b. Production of dyes
c. Pharmaceutical industry
d. Reagent in organic synthesis
e. Component in corrosion inhibitors
f. Ingredient in photographic developers

Toxicity

Considered toxic

Safety precautions

Exposure should be avoided

Check Digit Verification of cas no

The CAS Registry Mumber 4593-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4593-01:
(6*4)+(5*5)+(4*9)+(3*3)+(2*0)+(1*1)=95
95 % 10 = 5
So 4593-01-5 is a valid CAS Registry Number.

4593-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dibromo-3,6-dihydroxybenzene-1,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 4.5-Dibrom-3.6-dioxy-phthalsaeure-dinitril

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:4593-01-5 SDS

4593-01-5Relevant academic research and scientific papers

COMPOUND, PHOTOSENSITIVE RESIN COMPOSITION COMPRISING THE SAME, PHOTORESIST, COLOR FILTER AND DISPLAY DEVICE

-

Paragraph 0346-0347, (2020/12/30)

The present specification provides a compound represented by chemical formula 1 and a photosensitive resin composition including the same. A photosensitive material, a color filter and a display device are provided.

Routes to some 3,6-disubstituted phthalonitriles and examples of phthalocyanines derived therefrom. An overview

Heeney, Martin J.,Al-Raqa, Shaya A.,Auger, Aurélien,Burnham, Paul M.,Cammidge, Andrew N.,Chambrier, Isabelle,Cook, Michael J.

, p. 649 - 664 (2013/09/24)

The paper reviews a selection of synthetic pathways that provide access to 3,6-disubstituted phthalonitriles, precursors for the synthesis of 1,4,8,11,15,18,22,25-octasubstituted phthalocyanine derivatives. Early routes using Diels-Alder reactions for the

Synthesis, electrochemical, and photophysical studies of hexadecachlorinatedphthalocyaninato zinc(II)

Al-Raqa, Shaya Y.,Messali, Mouslim,Al-Refae, Saleem,Ghanem, Badr S.,Moussa, Ziad,Ahmed, Saleh,El-Khouly, Mohamed E.,Fukuzumi, Shunichi

experimental part, p. 231 - 236 (2012/02/03)

Synthesis of a new symmetrical 1,4,8,11,15,18,22,25-octahexyloxy-2,3,9,10, 16,17,23,24-octa-(3,5-dichlorophenyl)phthalocyaninato zinc(II), ZnPc, has been described and characterized by 1H NMR, 13C NMR, MS, UV-Vis, and IR spectrometry. The newly prepared ZnPc is soluble in organic solvents and is not aggregated in solution. The photophysical properties were studied by steady-state absorption and emission, cyclic voltammetry, and nanosecond transient absorption techniques. The prepared ZnPc absorbs and emits at longer wavelengths compared to that of reported phthalocyanine derivatives. The electron-donating properties of the ZnPc have been examined by mixing it with the electron-accepting dicyanoperylene-3,4,9,10-bis(dicarboximide), PDICN2. The recorded nanosecond transient spectra in the visible/near-IR region showed clearly the electron-transfer from the triplet-excited state of the ZnPc to PDICN2 with a rate of 3.40 × 108 M-1 s-1. Light absorption in a wide section of the solar spectrum, favorable redox properties, and the electron-transfer properties suggest usefulness of the ZnPc in light-energy harvesting and developing optoelectronic devices.

Novel synthesis of 1,4-dialkoxy-5,6,7,8-multisubstituted-2,3- dicyanonaphthalenes through electron transfer from Mg metal and efficient development of new naphthalocyanines

Miyazaki, Takeshi,Harada, Aiko,Maekawa, Hirofumi,Yamamoto, Yoshimasa,Nishiguchi, Ikuzo

experimental part, p. 862 - 868 (2011/06/28)

Novel methods for efficient synthesis of 1,4-diamyloxy-5,6,7,8- multisubstituted-2,3-dicyanonaphthalenes were successfully developed, starting from easily available 2,3-dicyanohydroquinone as a common single compound through only three steps, the first di

Phthalocyaninodehydroannulenes

Cook, Michael J.,Heeney, Martin J.

, p. 3958 - 3967 (2007/10/03)

4-Bromo- and 4,5-dibromo-3,6-dibutoxyphthalonitrile have been prepared and treated with 3,6-didecylphthalonitrile in cross tetramerisation reactions in the presence of nickel acetate to afford monobromo- and dibromo-dibutoxyhexadecylphthalocyaninato nicke

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