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1-(4-fluoronaphthyl)-3-(4-fluorophenyl)-2-propen-1-one is a complex organic compound with the molecular formula C17H10F2O. It is a derivative of chalcone, a type of ketone, characterized by the presence of two aromatic rings (naphthyl and phenyl) connected by a three-carbon chain with a double bond. The compound features two fluorine atoms, one attached to each aromatic ring, which may influence its electronic properties and reactivity. This chemical is primarily of interest in the field of organic chemistry, potentially for its use in the synthesis of pharmaceuticals, materials science, or as a precursor in the production of other complex molecules. Its specific applications and properties would depend on further research and development, as the compound's behavior in various chemical reactions and its potential benefits or drawbacks in practical applications are not detailed in this summary.

573-72-8

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573-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 573-72-8 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 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 573-72:
(5*5)+(4*7)+(3*3)+(2*7)+(1*2)=78
78 % 10 = 8
So 573-72-8 is a valid CAS Registry Number.

573-72-8Relevant academic research and scientific papers

Synthesis of new 3-(4-fluoronaphthyl)-5-(aryl)-2-isoxazolines and their antimicrobial and spermicidal activity

Sharma, Sharda,Pathak, Late V. N.,Madan, Harsha,Sharma, Arvind

scheme or table, p. 337 - 340 (2011/12/22)

Microwave assisted synthesis of 3-(4-fluoronaphthyl)-5-(aryl)-2- isoxazolines (3) from corresponding chalcones (2) and hydroxylamine hydrochloride has been accomplished. Structures of synthesized compounds have been confirmed on the basis of spectral studies (IR, 1H NMR) and analytical data. Representative compounds have been screened for their spermicidal activity in HF cattle and were also evaluated for their antibacterial activity against Staphylococcus aureus, E coli, Pseudomonas and antifungal activity against Candida albicans, Asperigillus niger, Fusarium oxysporum.

Solvent free synthesis of new-1-acetyl-3-(4-fluoronaphthyl)-5-substituted aryl pyrazolines as spermicides

Sharma, Sharda,Sharma, Arvind

scheme or table, p. 750 - 753 (2009/12/07)

In this paper we wish to report the solvent free synthesis of 1-acetyl-3-(4-fluoronaphthyl)-5-substituted aryl pyrazolines by using simple and efficient Green Chemistry techniques (Grindstone method and microwave irradiation). These methods have been developed for the rapid solvent free synthesis of title compounds from corresponding chalcones and hydrazine hydrate or phenylhydrazine in acetic acid. Considerable increase in the reaction rates have been observed with better yields compared with sample prepared from conventional method. Structure of synthesized new compounds have been confirmed on the basis of spectral (IR, 1H NMR) and analytical data. Representative compounds have been screened for their spermicidal activity in HF catties and Murrah buffalo.

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