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(Z)-methyl 3-((4-nitrophenyl)amino)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21880-93-3

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21880-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21880-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,8 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21880-93:
(7*2)+(6*1)+(5*8)+(4*8)+(3*0)+(2*9)+(1*3)=113
113 % 10 = 3
So 21880-93-3 is a valid CAS Registry Number.

21880-93-3Downstream Products

21880-93-3Relevant academic research and scientific papers

Encapsulating Au-Fe3O4 Nanodots into AIE-active Supramolecular Assemblies: Ambient Visible-light Harvesting “Dip-Strip” Photocatalyst for C?C/C?N Bond Formation Reactions

Kaur, Harpreet,Kaur, Mandeep,Walia, Preet Kamal,Kumar, Manoj,Bhalla, Vandana

, p. 809 - 813 (2019)

The present study demonstrates the development of a supramolecular porous ensemble consisting of hetero-oligophenylene derivative 6 and Au-Fe3O4 nanodots. Supramolecular assemblies of AIE-active hetero-oligophenylene derivative 6 served as reactors for the generation of Au-Fe3O4 nanodots. The as prepared supramolecular ensemble functioned as an efficient recyclable photocatalytic system for C(sp2)?H bond activation of anilines for the construction of quinoline carboxylates. Interestingly, the “dip catalyst” prepared by depositing PTh-co-PANI-6: Au-Fe3O4 nanodots on a filter paper served as a recyclable strip (up to 10 cycles) for C?C/C?N bond formation reaction.

Palladium-catalyzed oxidative coupling of aromatic primary amines and alkenes under molecular oxygen: Stereoselective assembly of (Z)-enamines

Ji, Xiaochen,Huang, Huawen,Wu, Wanqing,Li, Xianwei,Jiang, Huanfeng

, p. 11155 - 11162 (2013/12/04)

An efficient Pd-catalyzed oxidative coupling of aromatic primary amines and alkenes under molecular oxygen is disclosed. Under mild reaction conditions, it provides a rapid access to (Z)-enamine compounds with exceptional functional group tolerance and ex

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