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Hydrazinecarbothioamide, 2-(2,6-diphenyl-4-piperidinylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

502960-94-3

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502960-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 502960-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,9,6 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 502960-94:
(8*5)+(7*0)+(6*2)+(5*9)+(4*6)+(3*0)+(2*9)+(1*4)=143
143 % 10 = 3
So 502960-94-3 is a valid CAS Registry Number.

502960-94-3Upstream product

502960-94-3Relevant academic research and scientific papers

A facile microwave assisted green chemical synthesis of novel piperidino 2-thioxoimidazolidin-4-ones and their in vitro microbiological evaluation

Kanagarajan,Thanusu,Gopalakrishnan

, p. 67 - 77 (2011/10/17)

A series of novel hybrid heterocyclic compounds, 3-(3-alkyl-2,6- diarylpiperin-4-ylidene)-2-thioxoimidazolidin-4-ones were synthesised and a comparative study was also carried out under microwave irradiation. The synthesised compounds were characterised by their melting points, elemental analysis, MS, FT-IR, one-dimensional NMR (1H, D2O exchanged 1H and 13C), two dimensional HOMOCOSY and NOESY spectroscopic data. All the synthesised title compounds were screened for their in vitro antibacterial and antifungal activity against clinically isolated strains namely B. subtilis, M. luteus, S. typhii, S. paratyphii B, S. felxneri, P. vulgaris, A. niger, Mucor, Rhizopus and M. gypsuem and the results were discussed.

Synthesis and microbiological evaluation of novel [N-acetyl-2,6- diarylpiperidin-4-yl]-5-spiro-4-acetyl-2-(acetylamino)-Δ2-1,3, 4-thiadiazolines

Balasubramanian,Ramalingan,Aridoss,Parthiban,Kabilan

, p. 297 - 311 (2007/10/03)

Some novel spiropiperidinyl thiadiazolines have been synthesized and their bacterial activity against Streptococcus faecalis, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa and Klepsiella pneumoniae and antifungal activity against Cryptococcus neoformans, Candida-6, Candida-51, Aspergillus niger and Aspergillus flavus were evaluated. Compound 23 exhibited potent antibacterial activity in vitro against Klepsiella pneumoniae while compound 24 exerted potent antifungal activity in vitro against Cryptococcus neoformans. Birkhaeuser Boston 2004.

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