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1H-Isoindole-1,3(2H)-dione, 5,6-dichloro-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93296-62-9

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93296-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93296-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,9 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93296-62:
(7*9)+(6*3)+(5*2)+(4*9)+(3*6)+(2*6)+(1*2)=159
159 % 10 = 9
So 93296-62-9 is a valid CAS Registry Number.

93296-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dichloro-2-phenylisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 5,6-dichloro-2-phenyl-isoindoline-1,3-dione

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:93296-62-9 SDS

93296-62-9Relevant academic research and scientific papers

An efficient synthesis of N-substituted phthalimides using SiO2-tpy-Nb as heterogeneous and reusable catalyst

Wan, Li,Sun, Xiaoning,Shi, Songjie,Zhang, Jiawei,Li, Xin,Li, Zhenjiang,Guo, Kai

, p. 30 - 34 (2016/09/28)

A novel and efficient heterogeneous catalyst SiO2-tpy-Nb was developed, and its application in the preparation of N-substituted phthalimides from o-phthalic acids or anhydrides with amines provides the desired products in good to excellent yields. The catalyst was stable and recoverable for eight consecutive cycles without a significant loss in its activity. Furthermore, the catalyst is applicable in continuous flow which indicates its potential utilization in industrialization.

Process for the preparation of eight fluorine substituted phthalocyanine

-

, (2017/04/07)

The invention relates to a method for preparing octafluoro-substituted phthalocyanine. According to the method, easily available 4,5-dichlorophthalic acid serving as a raw material is subjected to five-step reactions, namely acetic anhydride dehydration, aniline imidization, potassium fluoride fluorination, hydrolysis and one-step condensation to obtain a target product, namely an octafluoro-substituted phthalocyanine compound. The method has the advantages of low raw material cost, mild reaction condition, safe experiment operation, simple post-treatment, relatively high target product yield, high purity and the like. A novel method is provided to preparation for synthesizing octafluoro-substituted phthalocyanine compounds, synthesis researches of octafluoro-substituted phthalocyanine compounds are promoted, and more possibility is provided to application of the octafluoro-substituted phthalocyanine compounds serving as semiconductor materials in researches of dye-sensitized solar cells, organic thin-film transistors and other aspects. The method can be easily industrialized, and the obtained product has high purity and stable quality.

Cyclic imides; 15. Reaction of 4,5-dichlorophthalimides with potassium nitrite: Synthesis of 4-hydroxy-nitrophthalimides

Caswell,Guevara,Corley,Martinez,Hollis,Largess,Thornley

, p. 823 - 825 (2007/10/02)

N-Substituted 4,5-dichlorophthalimides react with potassium nitrite in refluxing dimethylformamide to form N-substituted 4-hydroxy-5-nitrophthalimides.

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