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(E)-ethyl 3-(1'-(4''-methoxyphenyl)-3'-(3''',4'''-dimethoxyphenyl)-1'H-pyrazol-4'-yl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1236289-19-2

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1236289-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1236289-19-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,2,8 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1236289-19:
(9*1)+(8*2)+(7*3)+(6*6)+(5*2)+(4*8)+(3*9)+(2*1)+(1*9)=162
162 % 10 = 2
So 1236289-19-2 is a valid CAS Registry Number.

1236289-19-2Relevant academic research and scientific papers

Synthesis and in vitro biological evaluation of novel pyrazole derivatives as potential antitumor agents

Christodoulou, Michael S.,Fokialakis, Nikolas,Nam, Sangkil,Jove, Richard,Skaltsounis, Alexios-Leandros,Haroutounian, Serkos A.

, p. 779 - 788 (2012/10/29)

The synthesis of twenty seven novel pyrazole derivatives bearing aryl substituted groups at positions 1 and 3 of the pyrazole structural motif and various functional groups at position 4 is presented. The critical step for their synthesis is the TCT/DMF p

Novel pyrazole derivatives: Synthesis and evaluation of anti-angiogenic activity

Christodoulou, Michael S.,Liekens, Sandra,Kasiotis, Konstantinos M.,Haroutounian, Serkos A.

experimental part, p. 4338 - 4350 (2010/09/12)

The synthesis of a series of novel trisubstituted pyrazole derivatives and their PIFA-mediated conversion to molecules bearing the fused pyrazolo[4,3-c]quinoline ring system is reported. The anti-angiogenic activity of these compounds was evaluated by using in vitro assays for endothelial cell proliferation and migration, and in the chicken chorioallantoic membrane (CAM) assay. Compounds containing the fused pyrazolo[4,3-c]quinoline motifs emerged as potent anti-angiogenic compounds, which also had the ability to inhibit the growth of human breast (MCF-7) and cervical (Hela) carcinoma cells in vitro.

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