3046-94-4

Usage

Uses

Used in Chemical Industry:
2-(N-Butylanilino)ethanol is used as an intermediate substance or agent in the chemical industry for the synthesis of more complex chemical compounds. Its reactivity and versatility contribute to its utility in various chemical reactions and processes.
However, it is important to handle 2-(N-Butylanilino)ethanol with care to prevent exposure, ingestion, or inhalation, which could potentially cause harm. Due to insufficient data on its environmental and health impact, the potential risks and specific regulatory compliance for this chemical remain uncertain.

InChI:InChI=1/C12H19NO/c1-2-3-9-13(10-11-14)12-7-5-4-6-8-12/h4-8,14H,2-3,9-11H2,1H3

Upstream product

• 75-21-8 oxirane 
• 1126-78-9 N-(n-butyl)aniline 
• 109-65-9 1-bromo-butane 
• 122-98-5 2-Anilinoethanol 
• 87-72-9 D-Xylose 
• 23402-75-7 lithium di-tertbutyl cuprate 

Downstream Products

• 107778-81-4 N-butyl-N-(2-vinyloxy-ethyl)-aniline 
• 335672-84-9 N-butyl-N-[2-(methacryloyloxy)ethyl]aniline 
• 100966-13-0 N-(2-ethoxy-ethyl)-N-butyl-aniline 
• 860524-23-8 4-[butyl-(2-hydroxy-ethyl)-amino]-benzaldehyde 
• 335672-90-7 trans-2-n-butyl-2-[4-({4-[(5-methylisoxazol-3-yl-amino)sulfonyl]phenyl}diazenyl)phenylamino]ethyl methacrylate 
• 335672-99-6 trans-2-n-butyl-2-[4-({4-[(1,3-thiazol-2-ylamino)sulfonyl]phenyl}diazenyl)phenylamino]ethyl methacrylate 
• 103649-44-1 3-{4-[butyl-(2-hydroxy-ethyl)-amino]-benzylidenamino}-benzenesulfonic acid 
• 53817-39-3 N-butyl-N-(2-chloro-ethyl)-aniline 

Relevant academic research and scientific papers

Direct hydroxyethylation of amines by carbohydrates: Via ruthenium catalysis

An efficient and halogen-free catalytic methodology for the synthesis of β-amino alcohols from aromatic amines and biomass-derived carbohydrates is demonstrated for the first time. The activation of C5/C6 sugars by a ruthenium catalyst selectively generates the C2 alkylating reagent glycolaldehyde. The transformation involves metal-catalyzed hydrogen borrowing for the reduction of the imine intermediate. A series of arylamines bearing various substituents were successfully transformed into the desired products in good to excellent yields.

New photosensitive methacrylate monomers with 4-aminoazobenzene type chromophore group

Photosensitive methacrylate monomers, derivatives of azobenzene, were synthesized. The route of syntheses was based on coupling of diazonium salts of sulfathiazole, sulfomethoxazole, sulfadiazine, 4-aminobenzoic acid and 4-nitroaniline with N-alkyl-N-[2-(methacryloyloxy)ethyl]aniline. The trans?cis isomerization of the monomers in DMSO solution was investigated by UV-VIS spectroscopy recording their spectra during illumination and thermal recovery periods. It was found that except for nitro derivatives the yield of trans-cis isomerization was ca. 50% and that the reverse reaction was a result of thermal relaxation. The spectroscopic studies were accompanied by quantum chemical calculations.

Novel N-Alkylation of Amines with Organocopper Reagents

A mild and efficient method for the N-alkylation of amines is described, based on the oxidative coupling of lithium alkylcopper amide, which is derived from lithium dialkylcuprates and primary or secondary amines.The high chemospecificity of the method was demonstrated.