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(E)-6-methyl-8-(2,6,6-trimethylcyclohex-1-en-1-yl)oct-5-en-2-one is a complex organic compound characterized by its unique molecular structure. It is a conjugated dienone, which means it contains two carbon-carbon double bonds separated by a single carbon-carbon single bond. The compound features a cyclohexene ring with three methyl groups attached to it, contributing to its distinct chemical properties. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its reactive nature and ability to form stable intermediates in chemical reactions. Its structure also makes it a subject of interest in organic chemistry research, particularly in the study of reactions involving conjugated dienes and their applications in the formation of complex molecular architectures.

1150-17-0

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1150-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1150-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1150-17:
(6*1)+(5*1)+(4*5)+(3*0)+(2*1)+(1*7)=40
40 % 10 = 0
So 1150-17-0 is a valid CAS Registry Number.

1150-17-0Relevant academic research and scientific papers

Preparation method of vitamin A and vitamin A ester

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Paragraph 0019; 0065; 0068; 0073; 0076; 0081; 0084, (2020/04/02)

The invention provides a novel method for preparing vitamin A and vitamin A ester with farnesene as a raw material. The method comprises the following steps: reacting farnesene with acetoacetate underthe action of a catalyst to obtain farnesyl keto ester; carrying out a cyclization reaction and a dehydrogenation reaction on farnesene acetone, and then reacting a reaction product with vinyl magnesium halide to generate vinyl alcohol; carrying out a rearrangement reaction on vinyl alcohol to obtain vitamin A; and subjecting the vitamin A to an esterification reaction to obtain the vitamin A ester. The method avoids the defects of the existing processes, and the process line of the method is economical and effective.

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