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N-(4-fluoro-3-chlorophenyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1367992-25-3

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1367992-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1367992-25-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,7,9,9 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1367992-25:
(9*1)+(8*3)+(7*6)+(6*7)+(5*9)+(4*9)+(3*2)+(2*2)+(1*5)=213
213 % 10 = 3
So 1367992-25-3 is a valid CAS Registry Number.

1367992-25-3Downstream Products

1367992-25-3Relevant academic research and scientific papers

Ligand-free C-N bond formation in aqueous medium using a reusable Cu-Mn bimetallic catalyst

Sawant, Sanghapal D.,Srinivas, Mahesuni,Aravinda Kumar,Lakshma Reddy,Singh, Parvinder Pal,Singh, Baldev,Sharma, Amit Kumar,Sharma,Vishwakarma, Ram A.

, p. 5351 - 5354 (2013)

A general ligand-free protocol has been described for the recyclable and reusable Cu-Mn catalyzed C-N bond forming cross coupling reaction of arylboronic acids with various amines to form N-arylated amine products in aqueous medium affording excellent yields under ambient conditions, in 3-4 h.

Copper immobilized at a covalent organic framework: An efficient and recyclable heterogeneous catalyst for the Chan-Lam coupling reaction of aryl boronic acids and amines

Han, Yi,Zhang, Mo,Zhang, Ya-Qing,Zhang, Zhan-Hui

, p. 4891 - 4900 (2018/11/21)

A polyimide covalent organic framework (PI-COF) with high thermal and chemical stabilities has been readily prepared from commercially available and inexpensive reagents and was employed as an effective support for heterogeneous copper. It was demonstrated that the obtained Cu@PI-COF is a highly active heterogeneous catalyst which can effectively promote the Chan-Lam coupling reaction of aryl boronic acids and amines in an open flask without the aid of any base or additive. In addition, the catalyst could be readily recovered from the reaction mixture by simple filtration and reused for at least eight cycles without any observable change in structure and catalytic activity.

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