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4-fluoro-N-phenylnaphthalene-1-sulfonamide is a chemical compound with the molecular formula C16H12FNO2S. It is a derivative of naphthalene-1-sulfonamide, featuring a fluorine atom at the 4-position and a phenyl group attached to the nitrogen atom. 4-fluoro-N-phenylnaphthalene-1-sulfonamide is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its structure allows for the exploration of different chemical reactions and modifications, which can lead to the development of new therapeutic agents. The compound's properties, such as its solubility and reactivity, are influenced by the presence of the fluorine atom and the phenyl group, making it a subject of interest for researchers in medicinal chemistry.

571-54-0

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571-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 571-54-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 571-54:
(5*5)+(4*7)+(3*1)+(2*5)+(1*4)=70
70 % 10 = 0
So 571-54-0 is a valid CAS Registry Number.

571-54-0Relevant academic research and scientific papers

COMPOUNDS FOR BINDING PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 9 (PCSK9)

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Paragraph 0350, (2017/09/15)

The present disclosure relates to novel compounds, methods, and compositions capable of binding to PCSK9, thereby modulating PCSK9 proprotein convertase enzyme activity. The compounds of the disclosure include compounds Formula (I).

New compounds

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, (2008/06/13)

The present invention relates to substituted sulfonamide compounds of the general formula (I), wherein P is sulfonamide or amide-substituted sulfonic acid, which compounds are potentially useful for the prophylaxis and treatment of medical conditions relating to obesity, type II diabetes and/or disorders of the central nervous system.

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