20056-69-3

Upstream product

• 778630-63-0 1-(3-hydroxy-phenyl)-octan-1-one 
• 702660-60-4 1-(3-hydroxyphenyl)oct-1-ene 
• 234448-84-1 3-octylcyclohex-2-en-1-one 
• 17049-49-9 octylmagnesium bromide 
• 629-04-9 1-Bromoheptane 
• 13423-48-8 triphenylheptylphosphonium bromide 
• 603-35-0 triphenylphosphine 
• 1700-37-4 3-Benzyloxybenzaldehyde 
• 157888-43-2 8-(3-hydroxyphenyl)octanal 
• 5813-86-5 m-methoxybenzamide 
• 136116-43-3 1-(m-methoxyphenyl)-1-octanone 
• 13125-66-1 n-heptylmagnesium bromide 

Downstream Products

• 702660-66-0 2-hydroxy-4-n-octylbenzaldehyde 

Relevant academic research and scientific papers

Ozonization of phenols from Anacardium occidentale (cashew)

The phenolic lipid components cardanol and cardol, obtained from heat-processed technical cashew nutshell liquid from Anacardium occidentale, and anacardic acid from the natural product, each containing monoene, diene, and triene constituents, were ozoniz

Synthesis and antinematodal activity of 3-n-alkylphenols

Several 3-alkylphenols including 3-undecylphenol, which was isolated from a Sumatran rainforest plant, were synthesized to investigate their antinematodal activity against the phytopathogenic nematodes, Bursapherencus xylophilus. A three-step synthesis involving the treatment of 2-cyclohexen-1-one with the Grignard reagent, oxidation of the resulting 1-alkyl-2-cyclohexen-1-ol and subsequent aromatization of 3-alkyl-2-cyclohexen-1-one successfully afforded such phenols. Among the 3-alkylphenols, 3-nonylphenol showed the highest activity, while 3-decylphenol and 3-undecylphenol also showed high activity.

The separation and synthesis of lipidic 1,2- and 1,3-diols from natural phenolic lipids for the complexation and recovery of boron

A study has been made of the semi-synthesis of 1,3-diols (anacardic alcohols) from natural phenolic lipid resources from Anacardium occidentale and Anacardium giganteum which have given C15 and C11 derivatives, respectively. An isomeric 1,3-diol (isoanacardic alcohol) has been obtained from cardanol separated from technical cashew nut-shell liquid. Homologous1,3-diols have been synthesised from a range of synthetic 2-alkyl-, 3-alkyl- and 4-alkylphenols and from 6-alkylsalicylic acids. The natural 1,2-diol, urushiol, from Rhus vernicifera has been purified. All these lipidic compounds have been studied for their complexation and the potential recovery of boron as boric acid.

Preparation of diphenolics

A process for the production of diphenolic compounds having a divalent bridge. A first disubstituted phenol is reacted with an aldehyde in the presence of a secondary amine and excess alcohol to form an ether intermediate. The ether intermediate is reacted with a phenol having an open ortho or para position to form a diphenolic.