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1H-Pyrrole-2,5-dione, 3-(4-methoxyphenyl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21724-94-7

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21724-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21724-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,2 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21724-94:
(7*2)+(6*1)+(5*7)+(4*2)+(3*4)+(2*9)+(1*4)=97
97 % 10 = 7
So 21724-94-7 is a valid CAS Registry Number.

21724-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenyl)-1-phenylpyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names -

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:21724-94-7 SDS

21724-94-7Relevant academic research and scientific papers

Palladium-catalyzed aerobic oxidative carbonylation of alkynes with amines: a general access to substituted maleimides

Yang, Ji,Liu, Jiawang,Jackstell, Ralf,Beller, Matthias

supporting information, p. 10710 - 10713 (2018/09/29)

A catalytic oxidative carbonylation reaction was developed for the synthesis of polysubstituted maleimides from alkynes and amines with air as a green oxidant. This novel transformation proceeds in the presence of palladium chloride without the need for expensive ligands or additives and has a broad substrate scope affording a variety of maleimides in good to high yields.

Palladium-catalyzed direct arylation of maleimides: A simple route to bisaryl-substituted maleimides

Jafarpour, Farnaz,Shamsianpour, Mitra,Issazadeh, Salumeh,Dorrani, Masoumeh,Hazrati, Hamideh

, p. 1668 - 1672 (2017/03/08)

Palladium-catalyzed direct arylation of maleimides via Heck as well as organoboron-mediated Heck-type reactions are developed. These methods offer an approach to a wide variety of biologically interesting 3,4-diarylmaleimide scaffolds from readily accessible starting materials. These approaches led to the feasible one-pot construction of bisaryl-substituted maleimides which have historically been problematic.

Synthesis of 2-arylmaleimides via the Heck reaction

Roshchin, Alexander I.,Polunin, Evgeny V.

experimental part, p. 332 - 333 (2009/05/27)

The Heck reaction of maleimides with aryl iodides in the presence of PdCl2(MeCN)2, Bu4NCl and HCOOK affords the corresponding 2-arylmaleimides in moderate yields.

A facile synthesis of rubrolide E1

Kar, Anirban,Argade, Narshinha P.

, p. 2284 - 2286 (2007/10/03)

A simple and efficient synthesis of rubrolide E (1e) has been demonstrated via Meerwein coupling reaction of para-anisyldiazonium chloride with N-phenylmaleimide (2), regioselective reduction of para-anisylmaleic anhydride (4), Knoevenagel condensation of butyrolactone 5 with para-anisaldehyde and demethylation pathway. Georg Thieme Verlag Stuttgart.

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