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2-naphthalen-2-ylacetamide, also known as N-phenyl-2-naphthylamine, is an organic compound with the molecular formula C18H15NO. It is an antioxidant and ultraviolet stabilizer used in various materials, and has potential as an anti-cancer and anti-inflammatory agent.

36660-46-5

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36660-46-5 Usage

Uses

Used in Rubber and Plastics Industry:
2-naphthalen-2-ylacetamide is used as an antioxidant and ultraviolet stabilizer for protecting rubber, plastics, and other materials from degradation caused by exposure to sunlight and other environmental factors. It achieves this by scavenging free radicals and inhibiting polymer degradation.
Used in Pharmaceutical Research:
2-naphthalen-2-ylacetamide is used as a potential anti-cancer agent for its ability to inhibit the growth of certain types of cancer cells. It is also studied for its potential as an anti-inflammatory agent due to its capacity to reduce inflammation in animal models. However, further research is required to fully understand its biological and pharmacological properties and to explore its therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 36660-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36660-46:
(7*3)+(6*6)+(5*6)+(4*6)+(3*0)+(2*4)+(1*6)=125
125 % 10 = 5
So 36660-46-5 is a valid CAS Registry Number.

36660-46-5Relevant academic research and scientific papers

Palladium-catalyzed cyanomethylation of aryl halides through domino Suzuki coupling-isoxazole fragmentation

Velcicky, Juraj,Soicke, Arne,Steiner, Roland,Schmalz, Hans-Guenther

, p. 6948 - 6951 (2011)

A one-pot protocol for the cyanomethylation of aryl halides through a palladium-catalyzed reaction with isoxazole-4-boronic acid pinacol ester was developed. Mechanistically, the reaction proceeds through (1) Suzuki coupling, (2) base-induced fragmentation, and (3) deformylation as shown by characterization of all postulated intermediates. Under optimized conditions (PdCl2dppf, KF, DMSO/H2O, 130 °C) a broad spectrum of aryl bromides could be converted into arylacetonitriles with up to 88% yield.

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