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3-Cyclopentyl-1,3-diphenylpropan-1-one is a chemical compound with the molecular formula C21H22O. It is a white crystalline solid that belongs to the class of ketones, specifically a cycloalkyl ketone. 3-cyclopentyl-1,3-diphenylpropan-1-one is characterized by the presence of a cyclopentyl group attached to the third carbon of a propane-1-one backbone, with two phenyl groups attached to the first and third carbons. It is an organic compound with potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. The compound's properties, such as its melting point, solubility, and stability, can be influenced by the presence of the cyclopentyl and phenyl groups, making it an interesting target for further chemical research and development.

1669-76-7

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1669-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1669-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1669-76:
(6*1)+(5*6)+(4*6)+(3*9)+(2*7)+(1*6)=107
107 % 10 = 7
So 1669-76-7 is a valid CAS Registry Number.

1669-76-7Downstream Products

1669-76-7Relevant academic research and scientific papers

Visible-Light-Promoted Photocatalyst-Free Hydroacylation and Diacylation of Alkenes Tuned by NiCl2·DME

Zhao, Xinxin,Li, Bing,Xia, Wujiong

, p. 1056 - 1061 (2020/02/15)

Herein, we describe a visible light-promoted hydroacylation strategy that facilitates the preparation of ketones from alkenes and 4-acyl-1,4-dihydropyridines via an acyl radical addition and hydrogen atom transfer pathway under photocatalyst-free conditions. The efficiency was highlighted by wide substrate scope, good to high yields, successful scale-up experiments, and expedient preparation of highly functionalized ketone derivatives. In addition, this protocol allows for the synthesis of 1,4-dicarbonyl compounds through alkene diacylation in the presence of NiCl2·DME.

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