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2-(4-aminophenyl)-N-phenylacetamide is an organic compound with the chemical formula C14H14N2O. It is a derivative of acetamide, featuring a phenyl group attached to the nitrogen atom and a 4-aminophenyl group at the 2-position. 2-(4-aminophenyl)-N-phenylacetamide is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the development of drugs targeting the central nervous system. Its structure allows for the exploration of different chemical reactions and modifications, making it a valuable compound in medicinal chemistry research.

31733-44-5

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31733-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31733-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,3 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31733-44:
(7*3)+(6*1)+(5*7)+(4*3)+(3*3)+(2*4)+(1*4)=95
95 % 10 = 5
So 31733-44-5 is a valid CAS Registry Number.

31733-44-5Downstream Products

31733-44-5Relevant academic research and scientific papers

Pharmaceutical composition and method of treating cancer

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Page/Page column 45-46, (2020/12/07)

Cytotoxic compounds containing a phenyl core, amide link(s), an imidazolinone or a propenamide moiety. Also described are pharmaceutical compositions incorporating the cytotoxic compounds and methods for treating cancer. These compounds are cytotoxic against breast, prostate, and leukemia cancer cell lines via dual inhibition of Src kinases and tubulin.

Anticonvulsant activity of some 4-aminophenylacetamides

Clark,Davenport

, p. 18 - 20 (2007/10/02)

A series of 4-aminophenylacetamides was prepared and evaluated for anticonsulvant activity. These compounds were prepared during studies designed to determine the relationship between benzamide-like compounds and anticonsulvant effects. Unlike benzamides, these phenylacetamides have a methylene group between the aromatic ring and the amide carbonyl. Consequently, formal conjugation is lost, and the number of conformational degrees of freedom has increased. The compounds were tested in mice against seizures induced by electroshock and pentylenetetrazol, and in the rotorod assay for neurologic deficit. The more active and selective anticonsulvants prepared in this study were those having an additional aromatic ring as part of the substituent on the amide nitrogen. Compound 16, the 4-aminophenylacetamide derived from 2,6-dimethylaniline, was the most potent compound observed (ED50 = 50.50 mg/kg against electroshock-induced convulsions and ED50 = 93.20 mg/kg against pentylenetetrazol-induced convulsions).

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