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2,2,5,5-Tetramethyl-4-(3,4-dimethoxyphenylmethyl)hexan-3-one is a complex organic compound with the molecular formula C19H30O4. It is a white crystalline solid that is soluble in organic solvents. compound This is characterized by its unique structure, which includes four methyl groups attached to the central hexan-3-one backbone, and a 3,4-dimethoxyphenylmethyl group attached to the fourth carbon. The presence of the dimethoxyphenyl group gives it potential applications in the synthesis of pharmaceuticals and other organic compounds. Due to its specific functional groups and structural features, it may also be of interest in the field of materials science for the development of new polymers or other advanced materials.

80152-67-6

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80152-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80152-67-6 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 80152-67:
(7*8)+(6*0)+(5*1)+(4*5)+(3*2)+(2*6)+(1*7)=106
106 % 10 = 6
So 80152-67-6 is a valid CAS Registry Number.

80152-67-6Downstream Products

80152-67-6Relevant 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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