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4-Piperidinone, 1-hydroxy-2,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10604-77-0

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10604-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10604-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,6,0 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10604-77:
(7*1)+(6*0)+(5*6)+(4*0)+(3*4)+(2*7)+(1*7)=70
70 % 10 = 0
So 10604-77-0 is a valid CAS Registry Number.

10604-77-0Relevant academic research and scientific papers

Conformational analysis of some N- Hydroxypiperidin-4-one oximes

Baskar,Gopalakrishnan,Jabaraj, J. Winfred

experimental part, p. 580 - 584 (2009/12/26)

Analysis of the spectral data (1H NMR and 13C NMR) indicates that out of ten Af-hydroxypiperidin-4-one oximes 3a-j, the compounds 3b and 3c exist predominantly in chair conformation with the aryl and alky! substituents in the equator

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

Synthesis and in vitro microbiological evaluation of imidazo(4,5-b) pyridinylethoxypiperidones

Aridoss,Balasubramanian,Parthiban,Kabilan

, p. 268 - 275 (2007/10/03)

A series of imidazo(4,5-b)pyridinylethoxypiperidones was designed, synthesized and characterized for evaluation of potential antibacterial activity against Bacillus subtilis, Klebsiella pneumoniae, Escherichia coli, Staphylococcus aureus and Pseudomonas a

Synthesis and study of antibacterial and antifungal activities of novel 1-[2-(benzoxazol-2-yl)ethoxy]- 2,6-diarylpiperidin-4-ones

Ramalingan,Balasubramanian,Kabilan,Vasudevan

, p. 527 - 533 (2007/10/03)

Some novel benzoxazolylethoxypiperidones have been synthesized and their antibacterial activity against streptococcus faecalis, bacillus subtilis, escherichia coli, staphylococcus aureus aand pseudomonas aeruginosa and antifungal activity against Candida-6, Candida albicans, Aspergillus niger, Candida-51 and Aspergillus flavus were evaluated. Compounds 37, 38 and 39 exerted potent in vitro antibacterial activity against Streptococcus faecalis while compounds 40 and 41 exhibited potent in vitro antifungal activity against Candida-51.

Synthesis of some benzoxazolylethoxypiperidones

Ramalingan,Balasubramanian,Kabilan

, p. 187 - 192 (2007/10/03)

1-Hydroxy-2,6-diarylpiperidin-4-ones obtained from the corresponding 2,6-diarylpiperidin-4-ones upon cyanoethylation followed by condensation with o-aminophenol afforded 1-[2-(benzoxazol-2-yl)ethoxy]-2,6-diarylpiperidin-4-ones.

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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