60003-46-5

Usage

InChI:InChI=1/C14H20O3/c1-2-3-4-5-10-17-13-8-6-12(7-9-13)11-14(15)16/h6-9H,2-5,10-11H2,1H3,(H,15,16)

Upstream product

• 111-25-1 1-bromo-hexane 
• 15560-78-8 ethyl 2-(4-(n-hexyloxy)phenyl)acetate 
• 57792-40-2 1-(hexyloxy)-4-methylbenzene 
• 156-38-7 4-hydroxyphenylacetate 
• 5736-94-7 4-(hexyloxy)benzaldehyde 

Downstream Products

• 36935-45-2 4-Butyl-4'-hexyloxy-α-chlor-trans-stilben 
• 847749-10-4 (Pd(C₆H₃(O(CH₂)5CH₃)CHNC₆H₄O(CH₂)5CH₃)OCOCH₂C₆H₄O(CH₂)5CH₃)2 
• 847749-16-0 (Pd(C₆H₃(O(CH₂)9CH₃)CHNC₆H₄O(CH₂)9CH₃)OCOCH₂C₆H₄O(CH₂)5CH₃)2 

Relevant academic research and scientific papers

PROCESS FOR SYNTHESIZING PHENYLACETIC ACID BY CARBONYLATION OF TOLUENE

A production process for substituted phenylacetic acids or ester analogues thereof is disclosed. In this process toluene or toluene substituted with various substituents, an alcohol, an oxidant and carbon monoxide are used as raw materials to obtain compounds comprising structure of phenylacetic acid ester or analogues thereof by catalysis of the complex catalyst formed from transition metal and ligand, and such compounds are hydrolyzed to obtain various substituted phenylacetic acid based compounds. This type of compounds and their derivatives serve as important fine chemicals used widely in the industries of pharmaceuticals, pesticides, perfume and the like.

Efficient transformations of aldehydes and ketones into one-carbon homologated carboxylic acids

Peterson olefination of aldehydes and ketones with trimethylsilyl(methoxy)(benzotriazol-1-yl)methyl anion 6 afforded 1-(benzotriazol-1-yl)-1-methoxyalk-1-enes 7 which were treated without isolation with zinc bromide and hydrochloric acid, to yield the corresponding one-carbon homologated carboxylic acids 4 in good overall yields.

3-Arylcyclohex-2-en-1-ones and 2,6-Diarylcyclohex-2-en-1-ones. New Liquid Crystalline Compounds

The cyclohex-2-en-1-one unit flanked by one or more aryl rings is shown to provide a new system which can exhibit liquid crystal properties; these new mesogens contain a chiral centre which is both adjacent to a lateral dipolar carbonyl group and its also located in the central core.