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3-(2-hydroxybenzylidene)chroman-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30301-28-1

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30301-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30301-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,0 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30301-28:
(7*3)+(6*0)+(5*3)+(4*0)+(3*1)+(2*2)+(1*8)=51
51 % 10 = 1
So 30301-28-1 is a valid CAS Registry Number.

30301-28-1Relevant academic research and scientific papers

Coumarin-Based Bioactive Compounds: Facile Synthesis and Biological Evaluation of Coumarin-Fused 1,4-Thiazepines

Khoobi, Mehdi,Foroumadi, Alireza,Emami, Saeed,Safavi, Maliheh,Dehghan, Gholamreza,Alizadeh, Babak H.,Ramazani, Ali,Ardestani, Sussan K.,Shafiee, Abbas

, p. 580 - 586 (2012/05/04)

As part of our ongoing studies on the synthesis of bioactive coumarin compounds, we synthesized a series of new coumarin-fused 1,4-thiazepines using a simple method. The biological activity of target compounds along with 3-(2-hydroxybenzylidene)chroman-2,4-dione intermediates was screened by evaluation of their antioxidant and cytotoxic activities. The antioxidant activity was assessed using two methods, namely, 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging method and ferric reducing antioxidant power (FRAP) assay. 4-Methoxyphenolic compound 5d in thiazepine series showed the most potent scavenging activity, while the 4-bromophenolic derivative 5b was the most efficient compound in FRAP assay. Also, the result of cytotoxic evaluation using MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay demonstrated that compound 5b is at least twofold more potent than etoposide against MCF-7, SK-N-MC, and MDA-MB 231 cell lines. A series of new coumarin-fused 1,4-thiazepines were synthesized using a simple method. The biological activities of target compounds were screened by evaluation of their antioxidant and cytotoxic activities.

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