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4-Piperidinone, 1-[2-(1H-benzimidazol-2-yl)ethoxy]-2,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

677007-33-9

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677007-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 677007-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,0,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 677007-33:
(8*6)+(7*7)+(6*7)+(5*0)+(4*0)+(3*7)+(2*3)+(1*3)=169
169 % 10 = 9
So 677007-33-9 is a valid CAS Registry Number.

677007-33-9Downstream Products

677007-33-9Relevant academic research and scientific papers

Synthesis and biological evaluation of novel benzimidazol/ benzoxazolylethoxypiperidone oximes

Balasubramanian, Srinivasan,Aridoss, Gopalakrishnan,Parthiban, Paramasivam,Ramalingan, Chennan,Kabilan, Senthamaraikannan

, p. 125 - 130 (2007/10/03)

Some novel benzimidazol/benzoxazolylethoxypiperidone oximes were synthesized and their antibacterial activity against Staphylococcus aureus (NCIM-2492), Bacillus subtilis (NCIM-2439), Escherichia coli (NCIM-2345) and Pseudomonas aeruginosa (NCIM-2035) and

A Convenient Synthesis of Novel 1-[2-(Benzimidazol-2-yl)ethoxy]-2,6-diarylpiperidin-4-ones

Ramalingan,Balasubramanian,Kabilan

, p. 1105 - 1116 (2007/10/03)

Upon the study of biological evaluation of benzazolylethoxypiperidones, an array of novel benzimidazolylethoxypiperidones were synthesized. 2,6-Diarylpiperidin-4-ones upon strategical N-hydroxylation, cyanoethylation followed by acid aided condensation wi

Synthesis and microbiological evaluation of benzimidazolylethoxypiperidones

Ramalingan,Balasubramanian,Kabilan,Vasudevan

, p. 26 - 40 (2007/10/03)

Some novel benzimidazolylethoxypiperidones were synthesized and their antibacterial activity against Streptococcus faecalis, Bacillus subtilis, Eschericia coli, Pseudomonas aeruginosa and Klepsiella pneumoniae and antifungal activity against Cryptococcus neoformans, Candida 6, Candida 51 , Aspergillus niger and Aspergillus flavus evaluated. Compounds 38 and 39 exerted potent in vitro antibacterial activity against Klepsiella pneumoniae, while, compounds 41 and 42 exhibited potent in vitro antifungal activity against Cryptococcus neoformans.

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