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N-phenyl-N-2-fluorophenylbenzamide is a synthetic organic compound with the molecular formula C19H14FNO. It is a derivative of benzamide, featuring a phenyl group attached to the nitrogen atom, and a 2-fluorophenyl group attached to the same nitrogen atom. N-phenyl-N-2-fluorophenylbenzamide is characterized by its potential applications in pharmaceutical research, particularly as a building block for the development of new drugs or as a chemical probe to study biological processes. The presence of the fluorine atom in the 2-position of the phenyl ring can influence the compound's reactivity, lipophilicity, and potential binding properties, making it an interesting candidate for medicinal chemistry studies.

386-16-3

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386-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 386-16-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 386-16:
(5*3)+(4*8)+(3*6)+(2*1)+(1*6)=73
73 % 10 = 3
So 386-16-3 is a valid CAS Registry Number.

386-16-3Downstream Products

386-16-3Relevant academic research and scientific papers

A simple copper-catalyzed synthesis of tertiary acyclic amides

Racine, Emilie,Monnier, Florian,Vors, Jean-Pierre,Taillefer, Marc

supporting information; experimental part, p. 2818 - 2821 (2011/07/09)

The N-arylation of aromatic and aliphatic secondary acyclic amides, known to be poor nucleophiles, has been accomplished using a simple and cheap copper catalytic system. The corresponding tertiary acyclic amides, which can be found in numerous biologically active compounds, have been obtained in good to excellent yields.

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