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25771-65-7

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25771-65-7 Usage

General Description

8-nitro-4-phenylquinoline is a chemical compound with the molecular formula C15H10N2O2. It is a member of the quinoline family and contains a nitro group and a phenyl group. 8-nitro-4-phenylquinoline has been studied for its potential pharmacological and biological properties, including its antimicrobial and antineoplastic activities. Some studies have also investigated its use as a fluorescent probe for detecting and studying biomolecules. Additionally, 8-nitro-4-phenylquinoline has been explored for its potential in organic synthesis and as a building block for the development of new pharmaceuticals and materials. Its structure and properties make it a versatile and potentially valuable compound in various scientific and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 25771-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25771-65:
(7*2)+(6*5)+(5*7)+(4*7)+(3*1)+(2*6)+(1*5)=127
127 % 10 = 7
So 25771-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H10N2O2/c18-17(19)14-8-4-7-13-12(9-10-16-15(13)14)11-5-2-1-3-6-11/h1-10H

25771-65-7Relevant articles and documents

2,9-dichloro-4,7-diphenyl-1,10 phenanthroline

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Paragraph 0005; 0009, (2016/10/10)

The invention relates to 2,9-dichloro-4,7-diphenyl-1,10 phenanthroline, which belongs to the technical field of synthesis of organic chemistry. A method comprises the steps of: firstly mixing and stirring 8-nitroquinoline with sulfuric acid, dropwise adding benzene while stirring, mixing SnCl2.2H2O with acetic acid, and then adding into the reaction mixture, after stirring and mixing, inflating nitrogen gas, stirring, rising temperature, performing heat preservation, cooling to room temperature, dropwise adding sodium hydroxide under stirring, mixing with the acetic acid, adding potassium permanganate, stirring at constant temperature, adding benzoyl chloride, then slowly pouring the reaction mixture into icy water, introducing chlorine after stirring, sealing for reaction, and adding the sodium hydroxide, filtering, extracting filtrate and filtrate slag with hot benzene, combining the extract liquor, adding anhydrous sodium sulfate for drying, rotating to evaporate the benzene, and performing suction filtration. The invention has the beneficial effects of simple synthetic conditions, no secondary pollution, less side productions and a yield of more than 86%.

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