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

288303-40-2

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288303-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 288303-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,3,0 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 288303-40:
(8*2)+(7*8)+(6*8)+(5*3)+(4*0)+(3*3)+(2*4)+(1*0)=152
152 % 10 = 2
So 288303-40-2 is a valid CAS Registry Number.

288303-40-2SDS

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 4,5-dibromo-3,6-dibutoxybenzene-1,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 4,5-Dibromo-3,6-dibutoxyphthalonitrile

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:288303-40-2 SDS

288303-40-2Relevant academic research and scientific papers

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

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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