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2,2,6,6-Tetramethyl-5-(2,5-dimethoxyphenyl)heptan-3-one is a complex organic compound with the molecular formula C19H32O3. It is a ketone derivative, characterized by the presence of a carbonyl group (C=O) and a heptan-3-one structure, which means it has a seven-carbon chain with the ketone group at the third carbon. The compound features two methyl groups (CH3) at the 2nd and 6th positions of the heptane chain, and a 2,5-dimethoxyphenyl group attached at the 5th position. The dimethoxyphenyl group consists of a benzene ring with two methoxy groups (OCH3) at the 2nd and 5th positions. This chemical structure contributes to its unique properties and potential applications in various fields, such as pharmaceuticals or chemical research.

80152-61-0

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80152-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80152-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,5 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80152-61:
(7*8)+(6*0)+(5*1)+(4*5)+(3*2)+(2*6)+(1*1)=100
100 % 10 = 0
So 80152-61-0 is a valid CAS Registry Number.

80152-61-0Downstream Products

80152-61-0Relevant academic research and scientific papers

Substituent Effects in the Reaction of t-Butylmagnesium Chloride with Substituted Ethyl Cinnamates. A Correlation with 13C NMR Chemical Shifts

Jalander, Lars

, p. 419 - 428 (2007/10/02)

The reaction of t-butylmagnesium chloride with some substituted ethyl (E)-cinnamates gave mainly 1,3-, 1,4-, 1,2- and 1,4-addition products and minor amounts of 1,2- and 1,3-addition products.The relative amounts of 1,3-addition products has been shown to correlate with 13C NMR chemical shifts of C-α of the ethyl cinnamates.The correlation indicates that the regio selectivity of the reactions is to a great extent dependent of polar effects and that the t-butyl radical has a nucleophilic character.

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