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2-(benzotriazol-1-yl)-3-phenyl-2-propenenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

288071-94-3

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288071-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 288071-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,0,7 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 288071-94:
(8*2)+(7*8)+(6*8)+(5*0)+(4*7)+(3*1)+(2*9)+(1*4)=173
173 % 10 = 3
So 288071-94-3 is a valid CAS Registry Number.

288071-94-3Downstream Products

288071-94-3Relevant academic research and scientific papers

Synthesis and antitubercular activity of 3-aryl substituted-2-(1H(2H) benzotriazol-1(2)-yl)acrylonitriles

Sanna, Paolo,Carta, Antonio,Nikookar, Mohammad E. Rahbar

, p. 535 - 543 (2000)

A series of 223-aryl substituted-2-(1H(2H)-benzotriazol-1(2)- yl)acrylonitriles was synthesized for a preliminary in vitro evaluation of antitubercular activity according to an international program with the Tuberculosis Antimicrobial Acquisition and Coordinating Facility (TAACF). This work reports the synthetic approach and analytical and spectroscopic characterization (UV, IR, 1H- and 13C-NMR) of all compounds synthesized. Several compounds showed an interesting activity in the preliminary screening with a percent growth inhibition of the virulent Mycobacterium tuberculosis between 40 and 99% at the concentration of 12.5 μg/mL. The most effective derivatives E-5a and E-5e were also tested against M. avium in vitro. (C) 2000 Editions scientifiques et medicales Elsevier SAS.

New routes to the synthesis of pyridazinone, ethoxypyridine, pyrazole and pyrazolo[1,5-a]pyrimidine derivatives incorporating a benzotriazole moiety

Al-Omran,El-Hay,El-Khair

, p. 1617 - 1622 (2007/10/03)

A new approach to the synthesis of pyridazinone, ethoxypyridine, pyrazole and 7-aminopyrazolo-[1,5-a]pyrimidine derivatives. The structure of the newly synthesized compounds was elucidated by elemental analyses, ir, 1H nmr spectra and in some cases by 13C nmr investigations.

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