89765-17-3

Upstream product

• 64-67-5 diethyl sulfate 
• 93420-35-0 3-(p-hydroxyphenyl)-3-methyl-2-butanone 
• 77-78-1 dimethyl sulfate 
• 103-73-1 Phenetole 

Downstream Products

• 172045-78-2 1-(3-Phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpent-1-ene-3-one 
• 172045-82-8 1-(4-Fluoro-3-phenoxyphenyl)-3-chloro-4-(4-ethoxyphenyl)-4-methylpent-1-ene 
• 172045-80-6 1-(4-Fluoro-3-phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpent-1-ene-3-ol 
• 89764-65-8 1-(3-Phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpentane 
• 172045-79-3 1-(3-Phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpent-1-ene-3-ol 
• 172045-81-7 1-(3-Phenoxyphenyl)-3-chloro-4-(4-ethoxyphenyl)-4-methylpent-1-ene 
• 89764-44-3 1-[4-fluoro-3-phenoxy-phenyl]-4-[p-ethoxyphenyl]-4-methyl-pentane 
• 89765-18-4 1-(4-Fluoro-3-phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpent-1-ene-3-one 

Relevant academic research and scientific papers

Microwave-assisted Ketone-Ketone rearrangement: An improved synthesis of 3-(4-Alkoxyphenyl)-3-methylbutan-2-ones

(formula presented) A novel procedure for the preparation of 3-(4-alkoxyphenyl)-3-methylbutan-2-one in excellent yield is described via polymer-supported AlCl3-catalyzed rearrangement of 1-(4-ethoxyphenyl)-2,2-dimehtylpropan-1-one, followed by

Facile synthesis of 3-(p-alkoxyphenyl)-3-methyl-2-butanones

A novel procedure for the preparation of 3-(p-hydroxyphenyl)-3-methyl-2-butanone, in excellent yield, is described via a simple AlCl3 catalysed rearrangement of p-ethoxy-pivalophenone. Various 3-(p-alkoxyphenyl)-3-methyl-2-butanones have been s

Novel Synthesis and Insecticideal Activity of MTI-800, Desfluoro MTI-800 and Their Intermediates

A new route to the synthesis of 2-(4-ethoxyphenyl)-2-methyl-5-(3-phenoxyphenyl)pentane (desfluoro MTI-800) and 2-(4-ethoxyphenyl)-2-methyl-5-(4-fluoro-3-phenoxyphenyl)pentane (MTI-800) and the insecticidal activities of these compounds and some of the synthetic intermediates against the tobacco caterpillar Spodoptera litura (F.) is reported.

Certain aryl-alkane-2-pyridyloxy-phenyl derivatives having insecticidal and acaricidal activity

The present invention relates to novel aromatic alkane derivatives represented by the following general formula (I): STR1 wherein Ar stands for a substituted or unsubstituted phenyl or naphthyl group, R1 stands for a methyl, ethyl or isopropyl group and R2 stands for a hydrogen atom or a methyl group, or R1 and R2 together with the carbon to which they are attached jointly represent a substituted or unsubstituted cycloalkyl group and R3, stands for a fundamental group of an alcohol which is usually used in a form of R3 OH as to natural or synthetic pyrethroids, and also to the uses of these compounds. These compounds of the present invention have excellent insecticidal and acaricidal activities while the toxicities of these compounds are very low.