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3-(4-fluorophenyl)-1-(naphthalen-2-yl)prop-2-en-1-one is a complex organic chemical compound characterized by its unique molecular structure. It is a derivative of chalcone, a type of ketone, and features a naphthalene ring and a 4-fluorophenyl group attached to its prop-2-en-1-one backbone. 3-(4-fluorophenyl)-1-(naphthalen-2-yl)prop-2-en-1-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its diverse chemical properties. Its molecular formula is C18H13FO, and it has a molecular weight of 264.29 g/mol. The presence of the fluorine atom in the molecule can significantly influence its reactivity and physical properties, making it an interesting subject for further chemical research and development.

398-46-9

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398-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 398-46-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 398-46:
(5*3)+(4*9)+(3*8)+(2*4)+(1*6)=89
89 % 10 = 9
So 398-46-9 is a valid CAS Registry Number.

398-46-9Relevant academic research and scientific papers

Synthesis, Biological Activity and Action Mechanism Study of Novel Chalcone Derivatives Containing Malonate

Guo, Tao,Xia, Rongjiao,Liu, Tingting,Peng, Feng,Tang, Xuemei,Zhou, Qing,Luo, Hui,Xue, Wei

, (2020/03/13)

A series of novel chalcone malonate derivatives were synthesized and their antibacterial and antiviral activities were evaluated. All target compounds were characterized by spectral data. The results of antimicrobial bioassay showed that one compound (die

Synthesis and antimicrobial activities of new 4,6-diaryl- 4,5-dihydro-3-hydroxy-2H-indazoles

Amutha, Parasuraman,Nagarajan, Samuthira

experimental part, p. 428 - 432 (2012/06/30)

A series of new 4,6-diaryl-4,5-dihydro-3-hydroxy-2H-indazoles 5a-5k were synthesized by the cyclization of ethyl 2-oxo-4,6-diarylcyclohex-3-ene carboxylates 4a-4k. The compounds were characterized by IR, 1H NMR, 13C NMR, 2D NMR, and elemental analysis. The synthesized compounds were evaluated for in vitro antibacterial and antifungal activities against Staphylococcus aureus, Escherichia coli, Salmonella typhimurium, Pseudomonas aeruginosa, Candida albicans, Aspergillus niger, Aspergillus flavus, and Rhizopus sp. Most of the compounds exhibited good activity against the tested organisms. Copyright

Anti-bacterial and anti-leishmanial studies of 4, 6-diarylpyrimidin-2- amines

Bukhari, Mujahid Hussain,Siddiqui, Hamid Latif,Ashraf, Chaudhary Muhammad,Hussain, Tanvir

scheme or table, p. 720 - 725 (2012/06/18)

Seven new chalcones along with nine already reported ones were synthesized from aryl aldehydes and substituted acetophenones by Claisen-Schmidt condensation. Each chalcone was treated with guanidine hydrochloride followed by oxidation with H2O

Tetrachlorosilane-zinc chloride as a new potent binary reagent for one-pot, three-component synthesis of mannich-type products

Badawy, Doria S.,Abdel-Galil, Ebrahim,Kandeel, Ezzat M.,Basyouni, Wahid M.,Khatab, Tamer K.

experimental part, p. 2799 - 2812 (2010/04/03)

A combination of tetrachlorosilane and zinc chloride in dichloromethane as an efficient and ambient binary reagent to promote a one-pot amidoalkylation reaction of enolizable ketones, aromatic aldehydes with acetonitriles, or benzonitrile have been develo

Atom-efficient, solvent-free, green synthesis of chalcones by grinding

Rateb, Nora M.,Zohdi, Hussein F.

experimental part, p. 2789 - 2794 (2009/12/06)

An improved Claisen-Schmidt condensation reaction of methyl ketones and aromatic aldehydes can be achieved by grinding at room temperature in the absence of solvents. This process is simple, efficient, economical, and environmentally benign compared to classical reactions.

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