16260-10-9

Upstream product

• 104-43-8 4-dodecylphenol 
• 104-42-7 4-dodecylaniline 
• 143-15-7 1-dodecylbromide 
• 15890-72-9 laurylmagnesium bromide 
• 22161-92-8 1-dodecyl-4-methoxy-benzene 
• 696-62-8 para-iodoanisole 

Downstream Products

• 1428976-93-5 C₂₃H₃₈N₂O₃ 
• 1428976-92-4 C₂₃H₃₈N₂O₂ 
• 147637-88-5 Tris-(5-dodecyl-2-methoxy-phenyl)-amine 
• 147637-89-6 C₅₄H₈₇NO₃ 
• 147637-86-3 2-methoxy-4-dodecylaniline 
• 147637-87-4 4-Dodecyl-2-iodo-1-methoxy-benzene 
• 207462-05-3 1,8-bis(4-n-dodecyl-2-nitrophenoxy)-3,6-dioxaoctane 
• 147637-85-2 4-dodecyl-2-nitroanisole 
• 62529-18-4 4-dodecyl-2-aminophenol 

Relevant academic research and scientific papers

Direct asymmetric aldol reaction co-catalyzed by amphiphilic prolinamide phenol and lewis acidic metal on water

An approach based on combinations of various water compatible Lewis acids and lipophilic group containing amphiphilic prolinamide co-catalysts has been evaluated for the direct asymmetric Aldol reaction. From the broad screening of chloride salts from alk

Novel fluorescent quater- and quinquifurans: Syntheses and photophysical properties

In the quest for fast fluors for use in waveshifting polystyrene fibers, symmetrical oligofurans were investigated. Furan moieties were coupled by means of the Ullmann Reaction or by palladium-catalyzed unsymmetrical coupling; the latter gave higher yields. While the benzoxazole-terminated quater- and quinquifurans we prepared were both stable and fast, exhibiting a green fluorescence and decay times of about 2.4 nsec, they were inferior to other types of fluors in solubility and emission intensity when incorporated into polystyrene.

A Polar Globular Mesogen: Synthesis of a Tetrasubstituted Tribenzosilatrane

A tribenzosilatrane substituted with four alkyl tails has been synthesized in eight steps starting from p-alkylaniline with an overall yield of approximately 10percent; this molecular unit is designed for fabricating a new type of material where the overall globular shape can facilitate the obtainment of cubic symmetry mesophases; the use of different side chains could also yield macrochiral centres.

Certain benzoxazoles and the use thereof as metal extractants

Benzoxazoles having the structure STR1 where R is hydrogen or an alkyl group having from 1 to 20 carbon atoms, R' is hydrogen, chlorine or an alkyl group containing from 1 to 20 carbon atoms, X is H or Chlorine and the total number of carbon atoms in R an