14353-69-6

Usage

Uses

1. Used in NMR Probe Applications:
Benzenamine, N-hydroxy-2,4,6-trimethyl-, is used as a component in nuclear magnetic resonance (NMR) probe applications due to the presence of the mesityl group. The mesityl group's unique chemical properties and structure make it suitable for enhancing the sensitivity and accuracy of NMR spectroscopy, a powerful analytical technique used to determine the structure and properties of molecules.
2. Used in Chemical Synthesis:
The compound can also be utilized as a starting material or intermediate in the synthesis of various organic compounds, particularly those involving the mesityl group. Its reactivity and functional groups make it a valuable building block for the development of new molecules with potential applications in pharmaceuticals, materials science, and other areas.
3. Used in Research and Development:
Benzenamine, N-hydroxy-2,4,6-trimethyl-, can be employed in research and development for studying the properties and behavior of compounds containing the mesityl group. This can lead to a better understanding of the structure-activity relationships and the development of new compounds with improved properties and applications.

Upstream product

• 603-71-4 nitromesitylene 
• 14872-62-9 2,4,6-trimethyl-2'-nitro-1,1'-biphenyl 

Downstream Products

• 49839-60-3 C₁₁H₁₆N₂OS 
• 49839-67-0 C₁₁H₁₆N₂OS 
• 107341-60-6 N-(2,4,6-Trimethylphenyl)propylidenamin-N-oxid 
• 88-05-1 2,4,6-trimethylaniline 
• 39201-71-3 2,2',4,4',6,6'-hexamethylazoxybenzene 
• 2243-89-2 2,4,6-trimethylquinoline 
• 5692-66-0 2,2',4,4',6,6'-hexamethylazobenzene 
• 49839-57-8 C₁₈H₂₂N₂OS 
• 72725-84-9 4-nitro-benzaldehyde-(N-mesityl oxime ) 
• 1196-12-9 2-nitrosomesitylene 

Relevant academic research and scientific papers

Synthesis of meta-substituted anilines via copper-catalyzed [1,3]-methoxy rearrangement

meta-Substituted anilines were efficiently synthesized via copper-catalyzed [1,3]-methoxy rearrangement of N-methoxyanilines followed by Michael addition of nucleophiles to the in situ generated ortho-quinol imine. The present reaction exhibits excellent

Monomer-Dimer Solution Equilibria of 2,4,6-Trialkylnitrosobenzenes and 2,4,6-Trialkylnitrosobenzene/Nitrosobenzene Mixtures. A Study Using One- and Twodimensional NMR Techniques

2,4,6-Trimethylnitrosobenzene in CDCl3 exists as a mixture of monomer and Z- and E-azodioxy dimers.The dissociation kinetics of both dimers were measured by one-dimensional time-dependent NMR spectroscopy on non-equilibrium solutions, and by two-dimensional exchange spectroscopy (2D-EXSY) on equilibrium solutions. 2,4,6-Tri-t-butylnitrosobenzene is entirely monomeric in CDCl3 but forms mixed azodioxy dimers in the presence of nitrosobenzene.The dissociation kinetics of the mixed E-dimer were followed by NMR techniques.The activation energy parameters for these dissociation equilibria were compared with previous data on related nitrosobenzene and dimethylnitrosobenzene systems.