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2-(2-Methoxybenzyl)cyclopentanone is a chemical compound with the molecular formula C13H16O2. It is a derivative of cyclopentanone, featuring a 2-methoxybenzyl group attached to the 2-position of the cyclopentanone ring. 2-(2-methoxybenzyl)cyclopentanone is characterized by its aromatic and aliphatic components, with the methoxybenzyl group contributing a distinct smell and potentially influencing the compound's reactivity. It is often used in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and functional groups. The compound's properties, such as solubility and stability, can be influenced by the presence of the methoxy group, which can also affect its potential applications in chemical research and industry.

2866-63-9

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2866-63-9 Usage

Structure

Cyclopentanone ring with a 2-(2-methoxybenzyl) substituent attached

Classification

Ketone derivative

Usage

Organic synthesis, building block for pharmaceuticals and agrochemicals, flavoring agent in food, fragrance in perfumes

Chemical properties

Presence of methoxy group and benzyl moiety

Biological properties

Determined by the chemical structure and functional groups present in the molecule

Check Digit Verification of cas no

The CAS Registry Mumber 2866-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,6 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2866-63:
(6*2)+(5*8)+(4*6)+(3*6)+(2*6)+(1*3)=109
109 % 10 = 9
So 2866-63-9 is a valid CAS Registry Number.

2866-63-9Relevant academic research and scientific papers

Synthesis of chromans via Pd-catalyzed alkene carboetherification reactions

Ward, Amanda F.,Xu, Yan,Wolfe, John P.

supporting information; experimental part, p. 609 - 611 (2012/01/14)

A new method for the construction of 2-substituted and 2,2-disubstituted chromans via Pd-catalyzed carboetherification reactions between aryl/alkenyl halides and 2-(but-3-en-1-yl)phenols is described. These reactions effect formation of a C-O bond and a C-C bond to afford the chroman products in good yield, and also provide stereoselective access to tricyclic chroman derivatives.

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