6011-18-3

Basic information

• Product Name: Ethanone, 1-(3-aminophenyl)-, oxime (9CI)
• Synonyms: Ethanone, 1-(3-aminophenyl)-, oxime (9CI);3-Aminoacetophenone oxime
• CAS NO: 6011-18-3
• Molecular Formula: C₈H₁₀N₂O
• Molecular Weight: 150.1778
• Product Categories: AMINEPRIMARY
• Mol File: 6011-18-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 340.652°C at 760 mmHg
• Flash Point: 159.821°C
• Appearance: /
• Density: 1.15g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.564
• CAS DataBase Reference: Ethanone, 1-(3-aminophenyl)-, oxime (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3-aminophenyl)-, oxime (9CI)(6011-18-3)
• EPA Substance Registry System: Ethanone, 1-(3-aminophenyl)-, oxime (9CI)(6011-18-3)

Safety Data

• Hazardous Substances Data: 6011-18-3(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(3-aminophenyl)-, oxime (9CI) is a chemical compound that is also known by its chemical formula C8H10N2O. It is an oxime derivative and is typically used in the field of organic chemistry as a reagent for the synthesis of other compounds. It is also known to have potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications. Ethanone, 1-(3-aminophenyl)-, oxime (9CI) is of interest to researchers due to its unique structure and properties, which make it useful for a variety of chemical and biological applications. It is important to handle this compound with care, as it can pose potential hazards if not handled properly.

InChI:InChI=1/C8H10N2O/c1-6(10-11)7-3-2-4-8(9)5-7/h2-5,11H,9H2,1H3/b10-6+

Upstream product

• 106023-76-1 1-(3-Amino-phenyl)-ethanone O-allyl-oxime 
• 99-03-6 1-(3-aminophenyl)ethanone 
• 7471-32-1 m-nitroacetophenone oxime 

Downstream Products

• 129993-23-3 3-(1-Vinyl-1H-pyrrol-2-yl)-phenylamine 
• 134703-21-2 3‐(1H‐pyrrol‐2‐yl)aniline 
• 102-28-3 m-acetamide aniline 
• 75270-66-5 (CH₃)3SnONC(CH₃)C₆H₄NH₂ 
• 129725-48-0 α-(3-aminophenyl)ethylamine 
• 99-03-6 1-(3-aminophenyl)ethanone 

Relevant articles and documents

Copper-Catalyzed Three-Component Domino Cyclization for the Synthesis of 4-Aryl-5-(arythio)-2-(trifluoromethyl)oxazoles

A copper-catalyzed oxidative cyclization of oxime, arylthiol, and trifluoroacetic anhydride for the construction of trisubstituted oxazoles has been developed. This transformation combines N-O bond cleavage, C-H functionalization, and intramolecular annulation, providing a practical protocol for the introduction of a trifluoromethyl (-CF3) group at oxazole rings.

Synthesis of ketoximes via a solvent-assisted and robust mechanochemical pathway

A versatile and robust mechanochemical route to ketone-oxime conversions has been established for a broad range of ketones via a simple mortar-pestle grinding method. The relative reactivity of aldehydes vs. ketones under these conditions has also been explored, along with an examination of the possible connection between reactivity and electronic substituent effects.

Highly effective receptors showing di- vs. monosaccharide preference

Receptors 1 and 2, incorporating two heterocyclic recognition units as well as oxime- or hydroxymethyl-based hydrogen-bonding sites, were prepared, and their binding properties toward neutral sugars were determined. The design of these receptors was inspi