36588-31-5

Upstream product

• 693-58-3 1-Bromononane 
• 108-95-2 phenol 
• 139-02-6 sodium phenoxide 
• 693-03-8 n-butyl magnesium bromide 
• 109-72-8 n-butyllithium 

Downstream Products

• 39969-59-0 1-(4-nonyloxyphenyl)ethanone 
• 87734-53-0 1,5-Bis-(4-nonyloxy-phenyl)-pentane-1,5-dione 
• 101355-16-2 (2-bromo-phenyl)-nonyl ether 
• 105100-90-1 1-bromo-4-(nonyloxy)benzene 
• 95248-98-9 1-Chloro-4-nonyloxy-benzene 
• 95249-00-6 1-Chloro-2-nonyloxy-benzene 
• 124-11-8 non-1-ene 
• 108-95-2 phenol 
• 371112-64-0 1-(4-nonyloxyphenyl)-3-(4-undecyloxyphenylamino)prop-2-en-1-one 
• 371112-57-1 CH₃(CH₂)8OC₆H₄COCHCHNHC₆H₄O(CH₂)3CH₃ 
• 371112-63-9 CH₃(CH₂)8OC₆H₄COCHCHNHC₆H₄O(CH₂)9CH₃ 

Relevant academic research and scientific papers

Anionic cyclization of N -(trans -2,3-Diphenylaziridin-1-yl)imines: Its application to sesquiterpene synthesis via consecutive carbon-carbon bond-formation approach

The anionic consecutive carbon-carbon (CC-C) bond formation can be achieved by the anionic cyclizations of N-(trans-2,3-diphenylaziridin-1-yl)imines with alkyllithiums. The synthetic efficiency of CC-C bond-formation approach has been demonstrated in the synthesis of dl-pentalenene and dl-cedrone. Georg Thieme Verlag Stuttgart New York.

Effects of substituent branching and chirality on the physical properties of ionic liquids based on cationic ruthenium sandwich complexes

An appropriate understanding of how substituents affect the physical properties of ionic liquids is important for the molecular design of ionic liquids. Toward this end, we investigated how the branching and chirality of substituents affect the physical p

Liquid crystalline N-aryl-β-aminovinyl ketones and their complexes with lanthanides

Liquid crystalline lanthanide complexes with N-aryl-substituted β-aminovinyl ketones were synthesized for the first time. The complexes give rise to smectic A mesophase and are stable only in the solid state; in going to solution, they dissociate with for

Anionic reactions of N-(trans-2,3-diphenylaziridin-1-yl)imines and their use as 1,1-dipoles in anionic cyclizations

Reaction of N-(trans-2,3-diphenylaziridin-1-yl)imines with alkyllithiums and organocuprates afforded the desired addition products after consecutive fragmentations along with liberation of stilbene and nitrogen gas, while the reaction of N-(2-phenylaziridin-1-yl)imines under similar conditions gave an anomalous by-product. Anionic cyclizations of N-(trans-2,3-diphenylaziridin-1- yl)imines using unactivated alkenes and alkynes as acceptors proceeded smoothly, yielding cyclized products in good yields.