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1H-Pyrazole, 4,5-dihydro-5-(2-nitrophenyl)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

152192-62-6

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152192-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152192-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,1,9 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 152192-62:
(8*1)+(7*5)+(6*2)+(5*1)+(4*9)+(3*2)+(2*6)+(1*2)=116
116 % 10 = 6
So 152192-62-6 is a valid CAS Registry Number.

152192-62-6Relevant academic research and scientific papers

Anticancer activity of dihydropyrazolo[1,5-c]quinazolines against rat C6 glioma cells via inhibition of topoisomerase II

Kaur, Gagandeep,Cholia, Ravi P.,Joshi, Gaurav,Amrutkar, Suyog M.,Kalra, Sourav,Mantha, Anil K.,Banerjee, Uttam C.,Kumar, Raj

, (2018)

The design and synthesis of dihydropyrazolo[1,5-c]quinazolines (1a–h) as human topoisomerase II (TopoII) catalytic inhibitors are reported. The compounds were investigated for their antiproliferative activity against the C6 rat glial cell line. Two compou

Synthesis and xanthine oxidase inhibitory activity of 5,6-dihydropyrazolo/pyrazolo[1,5-c]quinazoline derivatives

Kumar, Deependra,Kaur, Gagandeep,Negi, Arvind,Kumar, Sanjeev,Singh, Sandeep,Kumar, Raj

, p. 57 - 64 (2015/01/08)

Some 5,6-dihydropyrazolo/pyrazolo[1,5-c]quinazoline derivatives were rationally designed, synthesized and evaluated for in vitro xanthine oxidase inhibitory activity for the first time. Some notions about structure activity relationships are presented. Th

Synthesis, characterization and in vitro antifungal evaluation of tetrahydropyrazolo[1,5-c]quinazolines

Insuasty, Braulio,Torres, Harlem,Quiroga, Jairo,Abonia, Rodrigo,Nogueras, Manuel,Sanchez, Adolfo,Sortino, Maximiliano,Zacchino, Susana,Low, John

, p. 153 - 160 (2007/10/03)

The synthesis of a series of new pyrazolo[1,5-c]quinazolines starting from 2-nitrobenzaldehyde is described. The structures of the obtained compounds were established by NMR and X-ray diffraction. In contrast with other quinazoline derivatives, these comp

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