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2,5-Pyrrolidinedione, 3-(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32856-95-4

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32856-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32856-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,5 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32856-95:
(7*3)+(6*2)+(5*8)+(4*5)+(3*6)+(2*9)+(1*5)=134
134 % 10 = 4
So 32856-95-4 is a valid CAS Registry Number.

32856-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-nitrophenyl)pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names p-Nitrophenyl-succinimid

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:32856-95-4 SDS

32856-95-4Relevant academic research and scientific papers

Selective and tunable synthesis of 3-arylsuccinimides and 3-arylmaleimides from arenediazonium tetrafluoroborates and maleimides

Yang, Zhen-Hua,Chen, Zhong-Hui,An, Yu-Long,Zhao, Sheng-Yin

, p. 23438 - 23447 (2016/03/12)

A highly efficient synthetic strategy for synthesizing 3-arylsuccinimides has been developed from arenediazonium tetrafluoroborates and maleimides in the presence of TiCl3. The reactions generated 3-arylsuccinimides in satisfactory yields under mild reaction conditions. In addition, 3-arylmaleimides were obtained by the coupling of arenediazonium tetrafluoroborate and maleimides catalyzed by CuCl. This methodology provided the selective and tunable synthesis of two classes of products by simply switching different metal reagents. The methods are simple, efficient and practical.

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