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2-Cyclopentyl-2-phenylacetamide is a chemical compound with the molecular formula C17H19NO. It is a white crystalline solid that is soluble in organic solvents. 2-cyclopentyl-2-phenylacetamide is a derivative of acetamide, featuring a cyclopentyl group and a phenyl group attached to the acetamide backbone. It is synthesized through the reaction of cyclopentylamine with phenylacetyl chloride. 2-Cyclopentyl-2-phenylacetamide has potential applications in the pharmaceutical industry, particularly as a building block for the development of new drugs, due to its unique structure and properties. However, further research is needed to explore its specific therapeutic potential and safety profile.

3900-94-5

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3900-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3900-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3900-94:
(6*3)+(5*9)+(4*0)+(3*0)+(2*9)+(1*4)=85
85 % 10 = 5
So 3900-94-5 is a valid CAS Registry Number.

3900-94-5Relevant academic research and scientific papers

Copper-Catalyzed Amide Radical-Directed Cyanation of Unactivated Csp3-H Bonds

Zhang, Hongwei,Zhou, Yulu,Tian, Peiyuan,Jiang, Cuiyu

supporting information, (2019/03/19)

A method for site-selective intermolecular δ/?-Csp3-H cyanation of aliphatic sulfonamides is developed using TsCN as the cyanating reagent, catalyzed by a Cu(I)/phenanthroline complex. The mild, expeditious, and modular protocol allows efficient remote Csp3-H cyanation with good functional group tolerance and high regioselectivity. Mechanistic studies indicate that the reaction might proceed through a Cu(I)-mediated N-F bond cleavage to generate an amidyl radical, 1,5-HAT, and cyano group transfer of the resulting carbon radical with TsCN.

ACID AND ESTER COMPOUNDS AND METHODS OF USING THE SAME

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Page/Page column 72-73, (2008/06/13)

Disclosed is a compound of having the formula (II-A), pharmaceutically acceptable salts or solvates thereof and pharmaceutical compositions containing the same, wherein the structural variables are as defined herein. The compounds, salts and solvates of this invention are useful as LXR agonists.

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