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2,2,6,6-Tetramethyl-5-(4-methoxyphenyl)heptan-3-one is a complex organic compound with the molecular formula C17H26O2. It is a colorless to pale yellow liquid with a molecular weight of 262.39 g/mol. 2,2,6,6-tetramethyl-5-(4-methoxyphenyl)heptan-3-one is characterized by its unique structure, featuring a heptanone backbone with four methyl groups at the 2, 2, 6, and 6 positions, and a 4-methoxyphenyl group attached at the 5th position. It is synthesized through various chemical reactions and is used in the fragrance and flavor industry due to its pleasant aroma. The compound is also known for its potential applications in the pharmaceutical sector, particularly as a precursor in the synthesis of certain drugs. Its chemical properties and reactivity make it a valuable compound for research and development in the field of organic chemistry.

80152-52-9

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80152-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80152-52-9 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, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80152-52:
(7*8)+(6*0)+(5*1)+(4*5)+(3*2)+(2*5)+(1*2)=99
99 % 10 = 9
So 80152-52-9 is a valid CAS Registry Number.

80152-52-9Downstream Products

80152-52-9Relevant 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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