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3,5-Dimethyl-1-oxo-cyclohex-2-en-6-carbonsaeure-aethylester, also known as 3,5-dimethyl-1-oxocyclohex-2-ene-6-carboxylic acid ethyl ester, is a complex organic compound with the chemical formula C11H16O3. It is a derivative of cyclohexane, featuring a cyclohexene ring with a carbonyl group at position 1, two methyl groups at positions 3 and 5, and a carboxylic acid group at position 6. The carboxylic acid is esterified with an ethyl group, making it an ethyl ester. 3,5-Dimethyl-1-oxo-cyclohex-2-en-6-carbonsaeure-aethylester is characterized by its unique structure and properties, which can be relevant in various chemical and industrial applications, such as the synthesis of fragrances, pharmaceuticals, or other specialty chemicals.

6102-16-5

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6102-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6102-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,0 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6102-16:
(6*6)+(5*1)+(4*0)+(3*2)+(2*1)+(1*6)=55
55 % 10 = 5
So 6102-16-5 is a valid CAS Registry Number.

6102-16-5Relevant academic research and scientific papers

Metal-Free I2-Catalyzed Highly Selective Dehydrogenative Coupling of Alcohols and Cyclohexenones

Liang, Yu-Feng,Yuan, Yizhi,Shen, Tao,Song, Song,Jiao, Ning

, p. 233 - 240 (2018)

The I2 catalyzed highly selective oxidative condensation of cyclohexenones and alcohols for the synthesis of aryl alkyl ethers has been described. DMSO is employed as the mild terminal oxidant. This novel methodology offers a metal-free reaction condition, operational simplicity and broad substrate scope to afford valuable products from inexpensive reagents. Various meta-substituted aromatic ethers which are hardly synthesized from the reported methods requiring meta-substituted phenols, are efficiently prepared by the present protocol.

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