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2,2,6,6-Tetramethyl-5-(2,6-dimethoxyphenyl)heptan-3-one is a complex organic compound with the molecular formula C19H32O3. It is a colorless to pale yellow liquid with a molecular weight of 308.46 g/mol. 2,2,6,6-tetramethyl-5-(2,6-dimethoxyphenyl)heptan-3-one is characterized by its unique structure, which includes a heptan-3-one backbone with four methyl groups at the 2, 2, 6, and 6 positions, and a 2,6-dimethoxyphenyl group attached at the 5 position. It is synthesized through a series of chemical reactions and is used in various applications, such as a fragrance ingredient and a chemical intermediate in the synthesis of other organic compounds. Due to its specific structure and properties, it is an important molecule in the field of organic chemistry and has potential applications in the pharmaceutical and chemical industries.

80152-64-3

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80152-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80152-64-3 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 80152-64:
(7*8)+(6*0)+(5*1)+(4*5)+(3*2)+(2*6)+(1*4)=103
103 % 10 = 3
So 80152-64-3 is a valid CAS Registry Number.

80152-64-3Downstream Products

80152-64-3Relevant 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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