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2-(4-(bromomethyl)phenyl)benzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53389-89-2

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53389-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53389-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,8 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53389-89:
(7*5)+(6*3)+(5*3)+(4*8)+(3*9)+(2*8)+(1*9)=152
152 % 10 = 2
So 53389-89-2 is a valid CAS Registry Number.

53389-89-2Downstream Products

53389-89-2Relevant academic research and scientific papers

Synthesis and antiacetylcholinesterase activity evaluation of new 2-aryl benzofuran derivatives

Pouramiri, Behjat,Mahdavi, Mohammad,Moghimi, Setareh,Firoozpour, Loghman,Nadri, Hamid,Moradi, Alireza,Tavakolinejad-Kermani, Esmat,Asadipour, Ali,Foroumadi, Alireza

, p. 897 - 902 (2016/10/31)

Starting from 2-hydroxybenzyl alcohol, a series of 2-arylbenzofurans have been synthesized and evaluated as acetylcholinesterase inhibitors at 23 μM by using modified colorimetric Ellman's method. The reaction sequence was completed in four steps. All of the fourteen synthesized products were obtained in excellent yields without the need to tedious work-up step. In the last step, different derivatives were obtained by the substitution of bromine with five and six-membered cyclic and acyclic amines. Among the synthesized compounds, the best activity was observed in 1-(4-(Benzofuran-2-yl) benzyl)piperidine 5c with 74% activity compared to donepezil as a reference drug.

Synthesis and calcium antagonistic activity of a series of diethyl benzofuryl, benzothienyl and benzogammapyronyl benzylphosphonates

Baziard-Mouysset, G.,Tchani, G. W.,Stigliani, J. L.,Payard, M.,Bonnafous, R.,Tisne-Versailles, J.

, p. 539 - 546 (2007/10/02)

In this work we present about 15 original heterocyclic diethyl benzylphosphonate analogues of fostedil, in which we have varied the nature of the heterocycle, the substituents or the phosphonic group, or even the position of this latter.Three diethyl 4-(2

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