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1-phenyl-3-pyridine-2-yl-1H-pyrazole-4-carboxaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

370098-30-9

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370098-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 370098-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,0,0,9 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 370098-30:
(8*3)+(7*7)+(6*0)+(5*0)+(4*9)+(3*8)+(2*3)+(1*0)=139
139 % 10 = 9
So 370098-30-9 is a valid CAS Registry Number.

370098-30-9Relevant academic research and scientific papers

Synthesis, antiviral, cytotoxicity and antitumor evaluations of A4 type of porphyrin derivatives

Fadda, Ahmed A.,El-Mekawy, Rasha E.,El-Shafei, Ahmed I.

, p. 753 - 768 (2015/10/29)

This manuscript describes the synthesis of a new series of porphyrin structures 4a-4m, 7, 9, 12 and 14. These structures were investigated against two types of viruses such as HIV-1 and HSV-1. Also they were screened for their antitumor activity. Among all tested compounds, it was found that compound 4b showed a high activity against HIV-1 and HSV-1 and against four different tumor cell lines. Most of the tested compounds showed a moderate degree of a potent antimicrobial activity. The structure of these compounds was confirmed on the basis of their analytical and spectral data such as UV-vis, IR, 13C NMR, 1H NMR spectroscopy and mass spectral data.

Synthesis, antiviral, cytotoxicity and antitumor evaluations of A4 type of porphyrin derivatives

Fadda, Ahmed A.,El-Mekawy, Rasha E.,El-Shafei, Ahmed I.

, p. 753 - 768 (2016/01/09)

This manuscript describes the synthesis of a new series of porphyrin structures 4a-4m, 7, 9, 12 and 14. These structures were investigated against two types of viruses such as HIV-1 and HSV-1. Also they were screened for their antitumor activity. Among all tested compounds, it was found that compound 4b showed a high activity against HIV-1 and HSV-1 and against four different tumor cell lines. Most of the tested compounds showed a moderate degree of a potent antimicrobial activity. The structure of these compounds was confirmed on the basis of their analytical and spectral data such as UV-vis, IR, 13C NMR, 1H NMR spectroscopy and mass spectral data.

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