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N-(3-fluoro-4-methylphenyl)benzamide is a chemical compound with the molecular formula C14H12FNO. It is a derivative of benzamide, featuring a 3-fluoro-4-methylphenyl group attached to the nitrogen atom. N-(3-fluoro-4-methylphenyl)benzamide is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and medicinal agents. Its structure provides a unique combination of electronic and steric properties, which can influence its reactivity and interactions with biological targets. The presence of a fluorine atom can significantly alter the physical and chemical properties of the molecule, such as its lipophilicity and metabolic stability, making it an interesting candidate for drug design.

456-89-3

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456-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 456-89-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 456-89:
(5*4)+(4*5)+(3*6)+(2*8)+(1*9)=83
83 % 10 = 3
So 456-89-3 is a valid CAS Registry Number.

456-89-3Downstream Products

456-89-3Relevant academic research and scientific papers

Palladium-Catalyzed Amide Synthesis via Aminocarbonylation of Arylboronic Acids with Nitroarenes

Peng, Jin-Bao,Li, Da,Geng, Hui-Qing,Wu, Xiao-Feng

supporting information, p. 4878 - 4881 (2019/06/17)

A palladium-catalyzed aminocarbonylation of aryl boronic acids with nitroarenes for the synthesis of amides has been developed. A wide range of substrates were well-tolerated and gave the corresponding amides in moderate to good yields. No external oxidant or reductant was needed in this procedure. This procedure provides a redox-economical process for the synthesis of amides.

Amide synthesis: Via nickel-catalysed reductive aminocarbonylation of aryl halides with nitroarenes

Cheung, Chi Wai,Leendert Ploeger, Marten,Hu, Xile

, p. 655 - 659 (2018/01/28)

Aminocarbonylation of aryl halides is one of the most useful methods in amide synthesis, but nitroarenes have not been used as a nitrogen source in this method even though they are more economical and accessible than anilines. Reported here is the development of nickel catalysis for the first three-component reactions of aryl halides, Co2(CO)8, and nitroarenes under reductive conditions to produce aryl amides. A wide range of (hetero)aryl iodides and bromides as well as nitro(hetero)arenes are suitable reaction partners, and high functional group compatibility has been achieved. The method might be used for the streamlined synthesis of aryl amides.

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