624-81-7

Usage

InChI:InChI=1/C2H7NO/c1-2-3-4/h3-4H,2H2,1H3

Upstream product

• 60-29-7 diethyl ether 
• 7119-91-7 2-bromo-2-nitroso-propane 
• 557-20-0 diethylzinc 
• 3585-94-2 4-nitro-benzaldehyd-(N-ethyl oxime ) 
• 7647-01-0 hydrogenchloride 
• 19207-59-1 N-ethyl-O-benzylhydroxylamine 
• 27430-64-4 N-ethyl-N-hydroxy-N'-phenyl-urea 
• 100391-47-7 ethyl-benzoyloxy-carbamic acid ethyl ester 
• 79-24-3 Nitroethane 
• 64-17-5 ethanol 
• 7664-93-9 sulfuric acid 

Downstream Products

• 49779-05-7 (Z)-N-(4-hydroxybenzylidene)ethanamine oxide 
• 26816-90-0 N-Aethyl-N-(m-chlor-phenylcarbamoyl)-hydroxylamin 
• 65616-26-4 N-benzyl-N-ethylhydroxylamine 
• 75-04-7 ethylamine 
• 7664-41-7 ammonia 
• 75-07-0 acetaldehyde 
• 64-19-7 acetic acid 
• 1217888-77-1 C₁₇H₁₆ClF₂N₇O₂ 
• 138708-87-9 bis-(1-ethyl-3-p-nitrophenyltriazene 1-oxide)nickel(II) 
• 101247-67-0 (S)-4-Methyl-2-(toluene-4-sulfonylamino)-pentanoic acid ethyl-hydroxy-amide 
• 101247-75-0 N-ethyl-6<(benzyloxycarbonyl)amino>caprohydroxamate 
• 101247-74-9 N-ethyl-4<(benzyloxycarbonyl)amino>butyrohydroxamate 
• 101247-73-8 N-ethyl-3<(benzyloxycarbonyl)amino>propiohydroxamate 
• 101247-72-7 3-(2-Chloro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl-hydroxy-amide 

Relevant academic research and scientific papers

Method for manufacturing ammonia-N

PROBLEM TO BE SOLVED: To provide a method for producing an N-alkyl hydroxylamine, which produces a pure N-alkyl hydroxylamine in a high yield under a mild condition by a simple method, does not require a strict time management and is advantageous for industrial-scale production. SOLUTION: The method for producing an N-alkyl hydroxylamine includes bringing an N-alkyl nitro compound into contact with a hydrogen source in the presence of a solid catalyst supporting palladium on silica and in the absence of a significant quantity of a fourth reaction component. The method for producing an N-alkyl hydroxylamine includes bringing (A) an N-alkyl nitro compound into contact only with (B) a hydrogen source and (C) a solid catalyst supporting palladium on silica, or bringing (A) an N-alkyl nitro compound into contact only with (B) a hydrogen source, (C) a solid catalyst supporting palladium on silica and (D) a solvent that does not deactivate catalytic activity and has a pKa of ≥12. COPYRIGHT: (C)2012,JPOandINPIT

Selective synthesis of N-Alkyl hydroxylamines by hydrogenation of nitroalkanes using supported palladium catalysts

The selective hydrogenation of nitroalkanes to the corresponding N-alkyl hydroxylamines is achieved at room temperature with excellent yields (up to 98 %), by using common supported palladium catalysts. The reaction temperature is key to the highly selective formation of the hydroxylamines, which proceeds smoothly in a H2 atmosphere without additives. The catalyst can be recycled up to five times.

The influence of preliminary treatment of Pt-Rh catalysts on their activity in transformations of nitroethane

The electrochemical reduction of nitroethane on electrochemically deposited Pt-Rh catalysts subjected to preliminary treatment under different conditions has been studied.The greatest increase in the specific activity of the electrochemical reduction as a result of the treatment is observed for rhodium and its alloys.

Catalytic Hydrogenation of Nitroethane at a Regulated Potential in the Presence of Palladium-Rhodium Catalysts

The influence of the potential on the rate, mechanism, and composition of the products of the catalytic hydrogenation of nitroethane in the presence of palladium-rhodium catalysts has been investigated.It is shown that, at a potential of 0.5 V, the reaction product is only ethylhydroxylamine.