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Pyridine, 2-[5-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-3-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

401513-95-9

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401513-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 401513-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,5,1 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 401513-95:
(8*4)+(7*0)+(6*1)+(5*5)+(4*1)+(3*3)+(2*9)+(1*5)=99
99 % 10 = 9
So 401513-95-9 is a valid CAS Registry Number.

401513-95-9Downstream Products

401513-95-9Relevant academic research and scientific papers

Synthesis, physicochemical properties, antimicrobial and antioxidant studies of pyrazoline derivatives bearing a pyridyl moiety

Lone, Imtiyaz Hussain,Khan, Khaliquz Zaman,Fozdar, Bharat Inder

, p. 363 - 369 (2014)

A series of new pyrazoline compounds bearing a pyridyl moiety (4a-i) were synthesized by condensing appropriate chalcones with hydrazine hydrate and tested for antimicrobial and antioxidant activities. According to in vitro antimicrobial activity against Bacillus subtilis, Staphylococcus epidermidis, Proteus vulgaris, Pseudomonas aeruginosa, Aspergillus niger and Penicillium chrysogenum and antioxidant activity by DPPH method, the compounds 4a, 4d, 4i and 4e, 4f, 4h showed maximum antimicrobial and antioxidant activities, respectively. Physiochemical properties and Lipinski's 'Rule of Five' analysis predicted higher intrinsic quality of the synthesized compounds and revealed that these compounds have good bioavailability and druglikeness properties.

Synthesis and antimycobacterial activity of 5-aryl-1-isonicotinoyl-3-(pyridin-2-yl)-4,5-dihydro-1H-pyrazole derivatives

Grazia Mamolo, Maria,Zampieri, Daniele,Falagiani, Valeria,Vio, Luciano,Banfi, Elena

, p. 593 - 599 (2007/10/03)

5-Aryl-1-isonicotinoyl-3-(pyridin-2-yl)-4,5-dihydro-1H-pyrazole derivatives were synthesized and tested for their in vitro antimycobacterial activity. The compounds showed an interesting activity against a strain of Mycobacterium tuberculosis and a human strain of M. tuberculosis H4.

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