16428-47-0

Usage

Uses

Used in Pharmaceutical Industry:
2-AMINO-1-(4-NITROPHENYL)ETHANOL is used as an intermediate in the synthesis of pharmaceuticals for its ability to facilitate the production of various organic compounds.
Used in Organic Synthesis:
2-AMINO-1-(4-NITROPHENYL)ETHANOL is used as a reagent in organic synthesis for the formation of esters and ethers, contributing to the development of a diverse range of chemical products.
Used in Antimicrobial Applications:
2-AMINO-1-(4-NITROPHENYL)ETHANOL is used as an antimicrobial agent for its antibacterial properties, making it a potential candidate for the development of new treatments against bacterial infections.
Used in Cancer Research:
2-AMINO-1-(4-NITROPHENYL)ETHANOL is used in the study of its potential application in cancer treatment due to its ability to inhibit certain enzymes involved in cancer cell growth, offering a promising avenue for future therapeutic advancements.
Used in Chemical Research:
2-AMINO-1-(4-NITROPHENYL)ETHANOL is used as a research compound to explore its properties and potential applications in various chemical processes, including the development of new methodologies and techniques in chemical synthesis.

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 18731-47-0 1-(4-nitrophenyl)-2-nitroethanol 
• 798-63-0 2-[2-(4-nitro-phenyl)-2-oxo-ethyl]-isoindole-1,3-dione 
• 92868-81-0 2-(2-hydroxy-2-(4-nitro-phenyl)-ethyl)-isoindole-1,3-dione 
• 99-81-0 4-Nitrophenacyl bromide 

Downstream Products

• 16428-47-0 (+) 2-amino-1-(4-nitro-phenyl)-ethanol 
• 103791-64-6 N-nicotinoyl-O-(3-pyridylcarbamoyl)-2-(4-nitrophenyl)-2-hydroxyethylamine 
• 103791-69-1 N,O-di(3-pyridylcarbamoyl)-2-(4-nitrophenyl)-2-hydroxyethylamine 
• 21719-25-5 N-(2-hydroxy-2-(4-nitrophenyl)ethyl)-4-methylbenzenesulfonamide 
• 69776-86-9 5-(4-nitrophenyl)oxazolidin-2-one 
• 82756-08-9 N-[2-Hydroxy-2-(4-nitro-phenyl)-ethyl]-oxalamic acid ethyl ester 
• 70547-97-6 N-(β-Hydroxy-β-p-nitrophenylethyl)-chloracetamid 
• 889140-50-5 5-chloro-1H-indole-2-carboxylic acid [2-hydroxy-2-(4-nitro-phenyl)ethyl]amide 
• 100427-74-5 3-<β-Hydroxy-β-(4-aminophenyl)ethylamino>quinuclidine 
• 103791-68-0 N,O-diphenylcarbamoyl-2-(4-nitrophenyl)-2-hydroxyethylamine 
• 103791-62-4 N-benzoyl-O-phenylcarbamoyl-2-(4-nitrophenyl)-2-hydroxyethylamine 
• 103791-71-5 N,O-di(4-pyridylcarbamoyl)-2-(4-nitrophenyl)-2-hydroxyethylamine 

Relevant academic research and scientific papers

Lewis acid mediated intramolecular C-O bond formation of alkanol-epoxide leading to substituted morpholine and 1,4-oxazepane derivatives: Total synthesis of (±)-Viloxazine

Substituted morpholines have been efficiently synthesised in good yields from nitrogen tethered alkanol-epoxide mediated by boron trifluoride etherate. The methodology has been used for the total synthesis of (±)-viloxazine.

Efficient preparation of biologically important 1,2-amino alcohols

An efficient three-step methodology developed for the preparation of 1,2-amino alcohols. In the first step a rapid coupling between bromoketones and potassium phthalimide in ionic liquid produced-phthalimido ketones in quantitative yields, which is followed by a facile reduction using NaCNBH 3 in acetic acid to give corresponding phthalimido alcohols and finally effecting hydrazinolysis in water at 60C to yield biologically important 1,2-amino alcohols.