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(E)-1-(4-(acridin-9-ylamino)phenyl)-3-(4-chlorophenyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1214741-02-2

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1214741-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1214741-02-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,7,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1214741-02:
(9*1)+(8*2)+(7*1)+(6*4)+(5*7)+(4*4)+(3*1)+(2*0)+(1*2)=112
112 % 10 = 2
So 1214741-02-2 is a valid CAS Registry Number.

1214741-02-2Relevant academic research and scientific papers

Green synthesis of some novel chalcone and isoxazole substituted 9-anilinoacridine derivatives and evaluation of their antimicrobial and larvicidal activities

Kalirajan,Mohammed Rafick,Sankar,Gowramma

, p. 583 - 590 (2019/05/21)

Synthesis of some novel 9-anilinoacridine derivatives 3a-j and 4a-j from 9-cloroacridine under MW irradiation have been reported. The structures of the synthesized compounds have been confirmed by physical and analytical data. The synthesized compounds have been screened for their in vitro anti-microbial activities against Staphylococcus aureus, Bacillus megaterium, Escherichia coli, Klebsiella pneumoniae, Candida albicans and Aspergillus Niger. Their larvicidal activity against Culex quinquefasciatus and Anopheles stephensi have also been screened by larval bioassay method. Many of the compounds have significant antimicrobial and larvicidal activities.

Docking studies, synthesis, characterization of some novel oxazine substituted 9-anilinoacridine derivatives and evaluation for their antioxidant and anticancer activities as topoisomerase II inhibitors

Kalirajan,Kulshrestha, Vivek,Sankar,Jubie

, p. 217 - 224 (2013/01/15)

A series of 9-anilinoacridines substituted with oxazine derivatives were synthesized to evaluate their antioxidant and anticancer activity against Daltons Lymphoma Ascites (DLA) cell growth by in vitro method. It was revealed that these conjugates exhibited significant antioxidant and anticancer activity (inhibition of DLA cell proliferation). Among these agents, compounds 5a, 5h, 5i, 5j were the most cytotoxic with CTC50 value of 140-250 μg/mL. The docking studies of the synthesized compounds were performed towards the key Topoisomerase II (1QZR) by using Schrodinger Maestro 9.2 version. The oxazine substituted 9-anilinoacridine derivatives 5a, 5h, 5i, 5j have significant anticancer activity as topoisomerase II inhibitors.

Synthesis of some novel pyrazole-substituted 9-anilinoacridine derivatives and evaluation for their antioxidant and cytotoxic activities

Kalirajan,Muralidharan,Jubie,Gowramma,Gomathy,Sankar,Elango

, p. 748 - 754 (2012/10/29)

This article focuses on the synthesis of new series of pyrazole-substituted 9-anilinoacridine derivatives 5a-m and 6a-l. The compounds were confirmed by physical and analytical data. The synthesized compounds when screened for in vitro antioxidant activity showed promising activity for many compounds. The selected compounds were screened for cytotoxic activity showed promising inhibition of HEp-2 cell line for the compounds 6c, 6e, and 6f.

Synthesis of new chalcone derivatives containing acridinyl moiety with potential antimalarial activity

Tomar,Bhattacharjee,Kamaluddin,Rajakumar,Srivastava, Kumkum,Puri

experimental part, p. 745 - 751 (2010/04/04)

A series of novel chalcones bearing acridine moiety attached to the amino group in their ring A have been synthesized through noncatalyzed nucleophilic aromatic substitution reaction between various 3′-aminochalcone or 4′-aminochalcones and 9-chloroacridine. The synthesized chalcone derivatives have been characterized and screened for in vitro antimalarial activity against Plasmodium falciparum NF-54. All the chalcones showed complete inhibition at concentration of 10 μg/mL and above while three compounds showed significant inhibition at concentration of 2 μg/mL. The three most active chalcone derivatives were screened for in vivo activity as well, but no significant inhibition in parasitaemia was observed when given intraperitoneally to Plasmodium yoelii infected mice model.

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