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N-[benzoylamino(ethyl)methyl]benzamide is a complex organic compound with the chemical formula C17H18N2O2. It is a derivative of benzamide, featuring a benzoyl group attached to an aminoethylmethyl moiety. N-[benzoylamino(ethyl)methyl]benzamide is characterized by its potential pharmaceutical applications, as it belongs to a class of molecules that can interact with biological targets, such as enzymes or receptors, in the human body. Its structure includes a central benzene ring with an amide group (-CO-NH2) and a substituted benzene ring attached through an amide linkage. The molecule's specific arrangement of atoms and functional groups may confer unique properties that are of interest in drug development, although further research would be required to explore its specific therapeutic potential and safety profile.

5202-75-5

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5202-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5202-75-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5202-75:
(6*5)+(5*2)+(4*0)+(3*2)+(2*7)+(1*5)=65
65 % 10 = 5
So 5202-75-5 is a valid CAS Registry Number.

5202-75-5Relevant academic research and scientific papers

Efficient synthesis of symmetrical bisamides from aldehydes and amides catalyzed by silica-bonded S-sulfonic acid nanoparticles

Tajbakhsh, Mahmood,Hosseinzadeh, Rahman,Alinezhad, Heshmatollah,Rezaee, Parizad

supporting information, p. 2370 - 2379 (2013/07/26)

Silica-bonded S-sulfonic acid nanoparticles (SBSSANPs) were easily synthesized from silica nanoparticles and showed to be an efficient catalyst in the synthesis the symmetrical N,N′-alkylidene bisamides. Reaction of aldehydes and amides in the presence of the catalyst afforded the corresponding bisamides in good to excellent yields. The extensive range of substrates suggests general applicability of the method. Reusability of the catalyst, simple workup procedure, and short reaction times are other advantages of this protocol. Copyright

Synthesis of 1-Aminoalkylphosphonic Acids via Amidoalkylation of Phosphorous Acid by N,N'-Alkylidenbisamides

Soroka, Miroslaw,Jaworska, Dorota,Szczesny, Zbigniew

, p. 1153 - 1155 (2007/10/02)

N,N'-Alkylidenebisamides 1, totally unsuitable as amidoalkylating agents toward phosphorous acid, react with its "activated" form prepared "in situ" from phosphorous(III) chloride and acetic acid to give the desired 1-amidoalkylphosphonic acids 2 in high yield.

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