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2,2,6,6-Tetramethyl-5-(3,5-dimethoxyphenyl)heptan-3-one is a complex organic compound with the molecular formula C18H30O3. It is a colorless to pale yellow liquid with a distinct aroma. 2,2,6,6-tetramethyl-5-(3,5-dimethoxyphenyl)heptan-3-one is known for its potential applications in the fragrance industry, where it can be used to create unique scents. It is also of interest in chemical research due to its structural properties. The compound is characterized by its heptan-3-one backbone, which is modified with four methyl groups and a 3,5-dimethoxyphenyl group, contributing to its stability and reactivity. It is synthesized through a series of chemical reactions and is typically handled with care due to its potential reactivity and the need for proper safety measures.

80152-70-1

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80152-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80152-70-1 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, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80152-70:
(7*8)+(6*0)+(5*1)+(4*5)+(3*2)+(2*7)+(1*0)=101
101 % 10 = 1
So 80152-70-1 is a valid CAS Registry Number.

80152-70-1Downstream Products

80152-70-1Relevant 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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