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2,2,5,5-Tetramethyl-4-(2,4,5-trimethoxyphenylmethyl)hexan-3-one is a complex organic compound with the molecular formula C20H32O5. It is a ketone derivative, characterized by the presence of a carbonyl group (C=O) and a long hydrocarbon chain. The compound features two methyl groups (CH3) at the 2nd and 5th positions of the hexan-3-one backbone, and a 2,4,5-trimethoxyphenylmethyl group attached to the 4th position. The trimethoxyphenylmethyl group consists of a phenyl ring with three methoxy groups (OCH3) at the 2nd, 4th, and 5th positions, and a methyl group (CH3) attached to the carbon atom. This unique structure endows the compound with specific chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science.

80152-74-5

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80152-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80152-74-5 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 80152-74:
(7*8)+(6*0)+(5*1)+(4*5)+(3*2)+(2*7)+(1*4)=105
105 % 10 = 5
So 80152-74-5 is a valid CAS Registry Number.

80152-74-5Downstream Products

80152-74-5Relevant 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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